ID

41025

Description

Study ID: 109275 Clinical Study ID: 109275 Study Title: An Open-Label, Single Sequence Study to Examine the Effects of Esomeprazole on the Pharmacokinetics of Orally Administered Lapatinib in Subjects with Metastatic ErbB2 Positive Breast Cancer Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: Lapatinib, Esomeprazole Trade Name: lapatinib plus esomeprazole Study Indication: Neoplasms, Breast

Keywords

Versions (2)
  1. 6/14/20 6/14/20 -
  2. 9/17/21 9/17/21 -
Copyright Holder

GlaxoSmithKline

Uploaded on

June 14, 2020

DOI

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License

Creative Commons BY-NC 4.0
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Effects of Esomeprazole on Lapatinib in Subjects with Breast Cancer; 109275

English

Screen

1 forms  
  1. StudyEvent: ODM
    1. Screen
Inform Screening
Description

Inform Screening

Alias
UMLS CUI-1
C0220908
Subject initials
Description

Clinical trial participant (person), Person Initials

Data type

text

Alias
UMLS CUI [1,1]
C1997894
UMLS CUI [1,2]
C2986440
Date of birth
Description

Patient date of birth

Data type

date

Alias
UMLS CUI [1]
C0421451
Inform Enrollment
Description

Inform Enrollment

Alias
UMLS CUI-1
C1516879
Subject number
Description

Clinical Trial Subject Unique Identifier

Data type

text

Alias
UMLS CUI [1]
C2348585
Date of Visit
Description

Date of Visit

Alias
UMLS CUI-1
C1320303
Date of visit/assessment
Description

Date of visit, Assessment Date

Data type

date

Alias
UMLS CUI [1,1]
C1320303
UMLS CUI [1,2]
C2985720
Demography
Description

Demography

Alias
UMLS CUI-1
C0011298
Date of birth
Description

Patient date of birth

Data type

date

Alias
UMLS CUI [1]
C0421451
Sex
Description

Gender

Data type

text

Alias
UMLS CUI [1]
C0079399
Ethnicity
Description

Ethnic group

Data type

text

Alias
UMLS CUI [1]
C0015031
Geographic ancestry
Description

Your ancestry or national origin

Data type

text

Alias
UMLS CUI [1]
C3841890
Eligibility Question
Description

Eligibility Question

Alias
UMLS CUI-1
C0013893
Did the subject meet all the entry criteria?
Description

Eligibility Determination

Data type

boolean

Alias
UMLS CUI [1]
C0013893
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI-1
C1512693
Histologically or cytologically confirmed diagnosis of: • Metastatic breast cancer that overexpresses ErbB2 (3+ by IHC, FISH, or CISH positive) OR • Recurrent, advanced, or metastatic solid tumor malignancy that is refractory to standard therapies, for which there is no approved therapy, and for which lapatinib in combination with one of the permitted anti-cancer regimens in the companion rollover protocol (EGF111767) may be suitable.
Description

Breast Carcinoma, Metastatic to, Estrogen receptor positive breast cancer; Malignant Neoplasms, Unresponsive to Treatment

Data type

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0036525
UMLS CUI [1,3]
C2938924
UMLS CUI [2,1]
C0006826
UMLS CUI [2,2]
C0205269
Is at least 18 years of age and not greater than 75 years of age.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
Is male or female.
Description

Gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
A female is eligible to enter and participate in the study if she is of: a. Non-childbearing potential (i.e. physiologically incapable of becoming pregnant), including any female who: • Has had a hysterectomy • Has had a bilateral oophorectomy (ovariectomy) • Has had a bilateral tubal ligation, or • Is post-menopausal (a demonstration of total cessation of menses for ≥ 1 year) or b. Childbearing potential, has a negative serum pregnancy test at Screening and agrees to one of the following:• Double-barrier contraception (condom with spermicidal jelly, foam, suppository, or film; diaphragm with spermicide; or male condom and diaphragm). • Complete abstinence from sexual intercourse from two weeks prior to administration of the study drug, throughout the active study treatment period, and two weeks post last administration of the study drug. • Vasectomized partner who is sterile prior to the female subject’s entry and is the sole sexual partner for that female.
Description

Childbearing Potential

Data type

boolean

Alias
UMLS CUI [1]
C3831118
Is able to swallow and retain oral medication.
Description

Oral medication, Able to swallow; Oral medication, Ability, Retained

Data type

boolean

Alias
UMLS CUI [1,1]
C0175795
UMLS CUI [1,2]
C2712086
UMLS CUI [2,1]
C0175795
UMLS CUI [2,2]
C0085732
UMLS CUI [2,3]
C0333118
ECOG performance status 0 to 2.
Description

ECOG Performance status

Data type

boolean

Alias
UMLS CUI [1]
C1520224
Adequate bone marrow function. • Hemoglobin ≥ 9 gm/dL (90g/L). • Absolute granulocyte count ≥ 1,500/mm3 (1.5 x 109/L). • Platelets ≥ 75,000/mm3 (75 x 109/L).
Description

Bone Marrow, physiological aspects

Data type

boolean

Alias
UMLS CUI [1,1]
C0005953
UMLS CUI [1,2]
C0031843
Calculated creatinine clearance (CrCl) ≥ 50 ml/min based on Cockcroft and Gault
Description

Estimation of creatinine clearance by Cockcroft-Gault formula

Data type

boolean

Alias
UMLS CUI [1]
C2711451
Total bilirubin ≤ 1.5 X upper limit of normal of institutional values.
Description

Bilirubin, total measurement

Data type

boolean

Alias
UMLS CUI [1]
C0201913
Alanine transaminase (ALT) ≤ 3 times the upper limit of the institutional values or ≤ 5 times ULN with documented liver metastases
Description

Alanine aminotransferase measurement

Data type

boolean

Alias
UMLS CUI [1]
C0201836
Has a left ventricular ejection fraction (LVEF) within the normal institutional range based on ECHO or MUGA.
Description

Left ventricular ejection fraction

Data type

boolean

Alias
UMLS CUI [1]
C0428772
Life expectancy of ≥ 12 weeks
Description

Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI-1
C0680251
Is pregnant or lactating.
Description

Pregnancy; Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
Has malabsorption syndrome, a disease affecting gastrointestinal function, or resection of the colon, stomach or small bowel.
Description

Malabsorption Syndrome; Disease, Affecting, gastrointestinal function; Colon resection; Stomach, Excision; Small intestine excision

Data type

boolean

Alias
UMLS CUI [1]
C0024523
UMLS CUI [2,1]
C0012634
UMLS CUI [2,2]
C0392760
UMLS CUI [2,3]
C0516983
UMLS CUI [3]
C4069040
UMLS CUI [4,1]
C0161898
UMLS CUI [4,2]
C0728940
UMLS CUI [5]
C0192601
Has current active hepatic or biliary disease (with exception of patients with Gilbert's syndrome, asymptomatic gallstones, liver metastases or stable chronic liver disease per investigator assessment)
Description

Liver diseases; Biliary System Disorder

Data type

boolean

Alias
UMLS CUI [1]
C0023895
UMLS CUI [2]
C3275124
Has evidence of symptomatic or uncontrolled brain metastases or leptomeningeal disease. Subjects with brain metastases treated by surgery and/or radiotherapy are eligible if neurologically stable and do not require steroids or anticonvulsants for at least 28 days prior to the first dose of study drug.
Description

Metastatic malignant neoplasm to brain; Leptomeningeal Neoplasms

Data type

boolean

Alias
UMLS CUI [1]
C0220650
UMLS CUI [2]
C0751297
Is considered medically unfit for the study by the investigator as a result of the medical interview, physical exam, or screening investigations.
Description

Medically unfit, Clinical Trials

Data type

boolean

Alias
UMLS CUI [1,1]
C3841806
UMLS CUI [1,2]
C0008976
Has a known immediate or delayed benzimidazole hypersensitivity reaction or idiosyncrasy to drugs chemically related to the investigational product such as gefitinib [Iressa] and erlotinib [Tarceva].
Description

Benzimidazole derivatives, antinematodal, Hypersensitivity; Experimental drug, Idiosyncrasy

Data type

boolean

Alias
UMLS CUI [1,1]
C3653457
UMLS CUI [1,2]
C0020517
UMLS CUI [2,1]
C0304229
UMLS CUI [2,2]
C0231191
Has a known hypersensitivity to esomeprazole.
Description

Esomeprazole, Hypersensitivity

Data type

boolean

Alias
UMLS CUI [1,1]
C0937846
UMLS CUI [1,2]
C0020517
Has received treatment with any investigational drug in the previous four weeks. (with the exception of lapatinib).
Description

Experimental drug, Previous

Data type

boolean

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0205156
Has received chemotherapy, immunotherapy, biologic therapy or hormonal therapy for the treatment of cancer within the past 14 days, with the exception of mitomycin C which is restricted for the past six weeks, and lapatinib. Subjects receiving lapatinib prior to study entry are eligible to participate in the study. NOTE: Any ongoing potentially reversible toxicity from prior anti-cancer therapy that is > Grade 1 or any toxicity from prior anti-cancer therapy that is progressing in severity will render the subject ineligible.
Description

Chemotherapy Regimen, Cancer treatment, Previous; Immunotherapy, Cancer treatment, Previous; Biological treatment, Cancer treatment, Previous; Hormone Therapy, Cancer treatment, Previous

Data type

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0920425
UMLS CUI [1,3]
C0205156
UMLS CUI [2,1]
C0021083
UMLS CUI [2,2]
C0920425
UMLS CUI [2,3]
C0205156
UMLS CUI [3,1]
C1531518
UMLS CUI [3,2]
C0920425
UMLS CUI [3,3]
C0205156
UMLS CUI [4,1]
C0279025
UMLS CUI [4,2]
C0920425
UMLS CUI [4,3]
C0205156
Is receiving any prohibited medication within the timeframe indicated on the prohibited medication list
Description

Pharmaceutical Preparations, prohibition

Data type

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0683610
Has physiological, familial, sociological, or geographical conditions that do not permit compliance with the protocol.
Description

Protocol compliance, Unpermitted

Data type

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C1299582
Has inadequate venous access for protocol-related blood draws.
Description

venous access, Inadequate (qualifier)

Data type

boolean

Alias
UMLS CUI [1,1]
C0750164
UMLS CUI [1,2]
C0205412
Clinically significant electrocardiogram (ECG) abnormality including baseline QTc prolongation >480msec, 2nd degree (type II), or 3rd degree AV block.
Description

ECG abnormality

Data type

boolean

Alias
UMLS CUI [1]
C1832603
History of sensitivity to heparin or heparin-induced thrombocytopenia.
Description

Heparin, Hypersensitivity; Heparin-induced Thrombocytopenia

Data type

boolean

Alias
UMLS CUI [1,1]
C0019134
UMLS CUI [1,2]
C0020517
UMLS CUI [2]
C0272285
Consumption of red wine, seville oranges, grapefruit or grapefruit juice and/or kumquats, pummelos, exotic citrus fruit (i.e. star fruit, bitter melon), grapefruit hybrids or fruit juices from seven days prior to the first dose of study medication.
Description

Red wine; Citrus aurantium; Grapefruit (food); GRAPEFRUIT JUICE

Data type

boolean

Alias
UMLS CUI [1]
C0349371
UMLS CUI [2]
C0330922
UMLS CUI [3]
C0995150
UMLS CUI [4]
C0452456
ECHO/MUGA
Description

ECHO/MUGA

Alias
UMLS CUI-1
C0013516
UMLS CUI-2
C0521317
Scan Type
Description

Echocardiography; Multiple gated acquisition scanning

Data type

text

Alias
UMLS CUI [1]
C0013516
UMLS CUI [2]
C0521317
Date and time of scan
Description

Echocardiography, Date in time, Time; Multiple gated acquisition scanning, Date in time, Time

Data type

datetime

Alias
UMLS CUI [1,1]
C0013516
UMLS CUI [1,2]
C0011008
UMLS CUI [1,3]
C0040223
UMLS CUI [2,1]
C0521317
UMLS CUI [2,2]
C0011008
UMLS CUI [2,3]
C0040223
Left ventricular ejection fraction (LVEF)
Description

Left ventricular ejection fraction

Data type

integer

Measurement units
  • %
Alias
UMLS CUI [1]
C0428772
%
Scan results
Description

Echocardiography, Result; Multiple gated acquisition scanning, Result

Data type

text

Alias
UMLS CUI [1,1]
C0013516
UMLS CUI [1,2]
C1274040
UMLS CUI [2,1]
C0521317
UMLS CUI [2,2]
C1274040
Describe abnormality
Description

Echocardiography, Result; Multiple gated acquisition scanning, Result

Data type

text

Alias
UMLS CUI [1,1]
C0013516
UMLS CUI [1,2]
C1274040
UMLS CUI [2,1]
C0521317
UMLS CUI [2,2]
C1274040
Medical Conditions
Description

Medical Conditions

Alias
UMLS CUI-1
C0012634
Does the subject have any current or past cancer or non-cancer related medical conditions?
Description

Disease

Data type

boolean

Alias
UMLS CUI [1]
C0012634
Sequence Number
Description

Disease, Sequence Number

Data type

integer

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C2348184
Specific Condition
Description

Disease

Data type

text

Alias
UMLS CUI [1]
C0012634
Modified Term
Description

Disease, Reported Term

Data type

text

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C2826302
MedDRA Synonym
Description

Disease, Medical Dictionary for Regulatory Activities Terminology (MedDRA), Synonym

Data type

text

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C1140263
UMLS CUI [1,3]
C0871468
MedDRA lower level term code
Description

Disease, MedDRA Low Level Term Code

Data type

text

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C3898442
Failed coding
Description

Disease, Code, Failed

Data type

text

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0805701
UMLS CUI [1,3]
C0231175
Status
Description

Disease, Status

Data type

text

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0449438
Disease Characteristics
Description

Disease Characteristics

Alias
UMLS CUI-1
C0599878
Tumour Classification at Initial Diagnosis
Description

primary tumor, Type - attribute, at initial diagnosis

Data type

text

Alias
UMLS CUI [1,1]
C0677930
UMLS CUI [1,2]
C0332307
UMLS CUI [1,3]
C4071762
Date of Initial Diagnosis
Description

Malignant Neoplasms, Diagnosis, Date in time

Data type

date

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0011900
UMLS CUI [1,3]
C0011008
Stage at Initial Diagnosis
Description

Malignant Neoplasms, Tumor stage, at initial diagnosis

Data type

text

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C1300072
UMLS CUI [1,3]
C4071762
Histology at Initial Diagnosis
Description

Malignant Neoplasms, Histology, at initial diagnosis

Data type

text

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0019638
UMLS CUI [1,3]
C4071762
Other, specify
Description

Malignant Neoplasms, Histology, at initial diagnosis

Data type

text

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0019638
UMLS CUI [1,3]
C4071762
ErbB2 (Her2/neu) Status ImmunoHisto-Chemistry (IHC)
Description

Malignant Neoplasms, HER2/Neu Status, Immunohistochemistry

Data type

text

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C1512413
UMLS CUI [1,3]
C0021044
Fluorescence in situ Hybridization (FISH)
Description

Malignant Neoplasms, Fluorescent in Situ Hybridization

Data type

text

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0162789
Date Metastatic Disease was First Diagnosed
Description

Neoplasm Metastatis, Date of Diagnosis

Data type

date

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C2316983
Abdomen/Abdominal Wall
Description

Neoplasm Metastasis, Abdomen; Neoplasm Metastasis, Abdominal wall structure

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0000726
UMLS CUI [2,1]
C0027627
UMLS CUI [2,2]
C0836916
Adrenals
Description

Neoplasm Metastasis, Adrenal Glands

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0001625
Bladder
Description

Neoplasm Metastasis, Urinary Bladder

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0005682
Blood
Description

Neoplasm Metastasis, Blood

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0005767
Bone
Description

Neoplasm Metastasis, Skeletal bone

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0262950
Bone Marrow
Description

Neoplasm Metastasis, Bone Marrow

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0005953
Breast
Description

Neoplasm Metastasis, Breast

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0006141
Cervix
Description

Neoplasm Metastasis, Cervix Uteri

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0007874
Chest Wall
Description

Neoplasm Metastasis, Chest wall structure

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0205076
CNS
Description

Neoplasm Metastasis, CNS metastases

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0686377
Colon
Description

Neoplasm Metastasis, Colon structure

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0009368
Esophagus/Oesophagus
Description

Neoplasm Metastasis, Esophagus

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0014876
Head and Neck
Description

Neoplasm Metastasis, Head and neck structure

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0460004
Heart
Description

Neoplasm Metastasis, Heart

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0018787
Kidney
Description

Neoplasm Metastasis, Kidney

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0022646
Liver
Description

Neoplasm Metastasis, Liver

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0023884
Lung
Description

Neoplasm Metastasis, Lung

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0024109
Lymph Nodes
Description

Neoplasm Metastasis, Lymph nodes

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0024204
Oral cavity
Description

Neoplasm Metastasis, Oral cavity

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0226896
Ovary
Description

Neoplasm Metastasis, Ovary

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0029939
Pancreas
Description

Neoplasm Metastasis, Pancreas

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0030274
Peritoneum
Description

Neoplasm Metastasis, Peritoneum

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0031153
Pleura
Description

Neoplasm Metastasis, Pleura

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0032225
Rectum
Description

Neoplasm Metastasis, Rectum

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0034896
Skin
Description

Neoplasm Metastasis, Skin

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C1123023
Small Intestine
Description

Neoplasm Metastasis, Intestines, Small

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0021852
Spleen
Description

Neoplasm Metastasis, Spleen

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0037993
Stomach
Description

Neoplasm Metastasis, Stomach

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0038351
Thyroid
Description

Neoplasm Metastasis, Thyroid Gland

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0040132
Other
Description

Neoplasm Metastasis, Other

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0205394
Please specify
Description

Neoplasm Metastasis, Other

Data type

text

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0205394
Prior Anti-Cancer Therapy
Description

Prior Anti-Cancer Therapy

Alias
UMLS CUI-1
C0920425
UMLS CUI-2
C1514463
Has the subject taken any prior cancer related therapy?
Description

Cancer treatment, Prior Therapy

Data type

boolean

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C1514463
Sequence Number
Description

Cancer treatment, Prior Therapy, Sequence Number

Data type

integer

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C1514463
UMLS CUI [1,3]
C2348184
Drug Name
Description

Cancer treatment, Prior Therapy, Medication name

Data type

integer

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C1514463
UMLS CUI [1,3]
C2360065
Modified reported term
Description

Cancer treatment, Prior Therapy, Reported term

Data type

text

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C1514463
UMLS CUI [1,3]
C2826302
GSK Drug synonym
Description

Cancer treatment, Prior Therapy, Synonym

Data type

text

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C1514463
UMLS CUI [1,3]
C0871468
GSK Drug Collection code
Description

Cancer treatment, Prior Therapy, Collection, Code

Data type

text

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C1514463
UMLS CUI [1,3]
C1516698
UMLS CUI [1,4]
C0805701
Failed coding
Description

Cancer treatment, Prior Therapy, Code, Failed

Data type

text

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C1514463
UMLS CUI [1,3]
C0805701
UMLS CUI [1,4]
C0231175
Therapy Type
Description

Cancer treatment, Prior Therapy, Type

Data type

text

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C1514463
UMLS CUI [1,3]
C0920425
Number of Cycles
Description

Cancer treatment, Prior Therapy, event cycle, Numbers

Data type

integer

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C1514463
UMLS CUI [1,3]
C1511572
UMLS CUI [1,4]
C0237753
Intent
Description

Cancer treatment, Prior Therapy, Intent

Data type

text

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C1514463
UMLS CUI [1,3]
C1283828
Start Date
Description

Cancer treatment, Prior Therapy, Start Date

Data type

date

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C1514463
UMLS CUI [1,3]
C0808070
Stop Date
Description

Cancer treatment, Prior Therapy, End Date

Data type

date

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C1514463
UMLS CUI [1,3]
C0806020
Best Response
Description

Cancer treatment, Prior Therapy, Best Overall Response

Data type

text

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C1514463
UMLS CUI [1,3]
C2986560
Cancer therapy treatment
Description

Cancer treatment, Prior Therapy

Data type

text

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C1514463
Anti-Cancer Radiotherapy
Description

Anti-Cancer Radiotherapy

Alias
UMLS CUI-1
C1522449
UMLS CUI-2
C0920425
Has the subject received any prior anti-cancer radiotherapy?
Description

Therapeutic radiology procedure, cancer treatment

Data type

boolean

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0920425
Sequence Number
Description

Therapeutic radiology procedure, cancer treatment, Sequence Number

Data type

integer

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0920425
UMLS CUI [1,3]
C2348184
Site
Description

Therapeutic radiology procedure, cancer treatment, Anatomic Site

Data type

text

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0920425
UMLS CUI [1,3]
C1515974
Cumulative Dose
Description

Therapeutic radiology procedure, cancer treatment, Cumulative Dose

Data type

text

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0920425
UMLS CUI [1,3]
C2986497
Units
Description

Therapeutic radiology procedure, cancer treatment, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0920425
UMLS CUI [1,3]
C1519795
Intent
Description

Therapeutic radiology procedure, cancer treatment, Intent

Data type

text

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0920425
UMLS CUI [1,3]
C1283828
Start Date
Description

Therapeutic radiology procedure, cancer treatment, Start Date

Data type

date

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0920425
UMLS CUI [1,3]
C0808070
Stop Date
Description

Therapeutic radiology procedure, cancer treatment, End Date

Data type

date

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0920425
UMLS CUI [1,3]
C0806020
Best Response
Description

Therapeutic radiology procedure, cancer treatment, Best Overall Response

Data type

text

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0920425
UMLS CUI [1,3]
C2986560
Cancer therapy treatment
Description

Therapeutic radiology procedure, cancer treatment

Data type

text

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0920425
Vital Signs
Description

Vital Signs

Alias
UMLS CUI-1
C0518766
Actual date/time
Description

Vital signs, Date in time, Time

Data type

datetime

Alias
UMLS CUI [1,1]
C0518766
UMLS CUI [1,2]
C0011008
UMLS CUI [1,3]
C0040223
Height
Description

Body Height

Data type

integer

Measurement units
  • cm
Alias
UMLS CUI [1]
C0005890
cm
Weight
Description

Body Weight

Data type

float

Measurement units
  • kg
Alias
UMLS CUI [1]
C0005910
kg
BMI
Description

Body mass index

Data type

float

Alias
UMLS CUI [1]
C1305855
Sitting heart rate
Description

heart rate while sitting

Data type

integer

Measurement units
  • bpm
Alias
UMLS CUI [1]
C2029904
bpm
Sitting blood pressure measurement - Systolic
Description

Systolic Pressure, Sitting position

Data type

integer

Measurement units
  • mmHg
Alias
UMLS CUI [1,1]
C0871470
UMLS CUI [1,2]
C0277814
mmHg
Sitting blood pressure measurement - Diastolic
Description

Diastolic blood pressure, Sitting position

Data type

integer

Measurement units
  • mmHg
Alias
UMLS CUI [1,1]
C0428883
UMLS CUI [1,2]
C0277814
mmHg
12-Lead ECG
Description

12-Lead ECG

Alias
UMLS CUI-1
C0430456
Date and Time of ECG
Description

12 lead ECG, Date in time, Time

Data type

datetime

Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C0011008
UMLS CUI [1,3]
C0040223
Heart rate
Description

12 lead ECG, Heart rate

Data type

integer

Measurement units
  • bpm
Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C0018810
bpm
PR Interval
Description

12 lead ECG, Electrocardiogram: P-R interval

Data type

integer

Measurement units
  • msec
Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C0429087
msec
QRS Duration
Description

12 lead ECG, QRS complex duration

Data type

integer

Measurement units
  • msec
Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C0429025
msec
Uncorrected QT Interval
Description

12 lead ECG, QT interval - finding

Data type

integer

Measurement units
  • msec
Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C1287082
msec
QTc Interval
Description

12 lead ECG, Electrocardiogram QT corrected interval

Data type

integer

Measurement units
  • msec
Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C0855331
Result of the ECG
Description

12 lead ECG, Result

Data type

text

Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C1274040
12-Lead ECG Abnormalities
Description

12-Lead ECG Abnormalities

Alias
UMLS CUI-1
C0430456
UMLS CUI-2
C1704258
Date and Time of ECG
Description

12 lead ECG, Abnormality, Date in time, Time

Data type

datetime

Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C1704258
UMLS CUI [1,3]
C0011008
UMLS CUI [1,4]
C0040223
Record clinically significant abnormalities
Description

12 lead ECG, Abnormality

Data type

text

Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C1704258
Randomization Number
Description

Randomization Number

Alias
UMLS CUI-1
C0034656
UMLS CUI-2
C0237753
Was the subject able to be randomized?
Description

Randomisation

Data type

boolean

Alias
UMLS CUI [1]
C0034656
Yes, provide Randomization number
Description

Randomisation, Numbers

Data type

integer

Alias
UMLS CUI [1,1]
C0034656
UMLS CUI [1,2]
C0237753
Yes, provide Date of randomization
Description

Randomization, Date in time

Data type

date

Alias
UMLS CUI [1,1]
C0034656
UMLS CUI [1,2]
C0011008
Local Laboratory - Clinical Chemistry
Description

Local Laboratory - Clinical Chemistry

Alias
UMLS CUI-1
C0022885
UMLS CUI-2
C0008000
Laboratory Used For This Sample
Description

Chemistry, Clinical, Laboratory

Data type

date

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0022877
Gender used to determine lab normals
Description

Chemistry, Clinical, Reference lab test reference range, Gender

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0883335
UMLS CUI [1,3]
C0079399
Date of birth used to determine lab normals
Description

Chemistry, Clinical, Reference lab test reference range, Patient date of birth

Data type

date

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0883335
UMLS CUI [1,3]
C0421451
Laboratory Used For This Sample
Description

Chemistry, Clinical, Laboratory

Data type

date

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0022877
Date sample taken
Description

Chemistry, Clinical, Sampling, Date in time

Data type

date

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0870078
UMLS CUI [1,3]
C0011008
Was the subject fasting for this laboratory?
Description

Chemistry, Clinical, Fasting

Data type

boolean

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0015663
Albumin
Description

Chemistry, Clinical, Albumin measurement

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201838
Albumin - Result
Description

Chemistry, Clinical, Albumin measurement, Result

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201838
UMLS CUI [1,3]
C1274040
Albumin - Units
Description

Chemistry, Clinical, Albumin measurement, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201838
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
Albumin - Low
Description

Chemistry, Clinical, Albumin measurement, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201838
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
Albumin - High
Description

Chemistry, Clinical, Albumin measurement, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201838
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
Albumin - Tox Grade
Description

Chemistry, Clinical, Albumin measurement, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201838
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
Alkaline Phosphatase
Description

Chemistry, Clinical, Alkaline phosphatase measurement

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201850
Alkaline Phosphatase - Result
Description

Chemistry, Clinical, Alkaline phosphatase measurement, Result

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201850
UMLS CUI [1,3]
C1274040
Alkaline Phosphatase - Units
Description

Chemistry, Clinical, Alkaline phosphatase measurement, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201850
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
Alkaline Phosphatase - Low
Description

Chemistry, Clinical, Alkaline phosphatase measurement, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201850
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
Alkaline Phosphatase - High
Description

Chemistry, Clinical, Alkaline phosphatase measurement, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201850
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
Alkaline Phosphatase - Tox Grade
Description

Chemistry, Clinical, Alkaline phosphatase measurement, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201850
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
ALT
Description

Chemistry, Clinical, Alanine aminotransferase measurement

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201836
ALT - Result
Description

Chemistry, Clinical, Alanine aminotransferase measurement, Result

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201836
UMLS CUI [1,3]
C1274040
ALT - Units
Description

Chemistry, Clinical, Alanine aminotransferase measurement, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201836
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
ALT - Low
Description

Chemistry, Clinical, Alanine aminotransferase measurement, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201836
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
ALT - High
Description

Chemistry, Clinical, Alanine aminotransferase measurement, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201836
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
ALT - Tox Grade
Description

Chemistry, Clinical, Alanine aminotransferase measurement, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201836
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
AST
Description

Chemistry, Clinical, Aspartate aminotransferase measurement

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201899
AST - Result
Description

Chemistry, Clinical, Aspartate aminotransferase measurement, Result

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201899
UMLS CUI [1,3]
C1274040
AST - Units
Description

Chemistry, Clinical, Aspartate aminotransferase measurement, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201899
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
AST - Low
Description

Chemistry, Clinical, Aspartate aminotransferase measurement, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201899
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
AST - High
Description

Chemistry, Clinical, Aspartate aminotransferase measurement, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201899
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
AST - Tox Grade
Description

Chemistry, Clinical, Aspartate aminotransferase measurement, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201899
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
Direct Bilirubin
Description

Chemistry, Clinical, Bilirubin, direct measurement

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201916
Direct Bilirubin - Result
Description

Chemistry, Clinical, Bilirubin, direct measurement, Result

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201916
UMLS CUI [1,3]
C1274040
Direct Bilirubin - Units
Description

Chemistry, Clinical, Bilirubin, direct measurement, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201916
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
Direct Bilirubin - Low
Description

Chemistry, Clinical, Bilirubin, direct measurement, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201916
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
Direct Bilirubin - High
Description

Chemistry, Clinical, Bilirubin, direct measurement, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201916
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
Direct Bilirubin - Tox Grade
Description

Chemistry, Clinical, Bilirubin, direct measurement, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201916
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
Total Bilirubin
Description

Chemistry, Clinical, Bilirubin, total measurement

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201913
Total Bilirubin - Result
Description

Chemistry, Clinical, Bilirubin, total measurement, Result

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201913
UMLS CUI [1,3]
C1274040
Total Bilirubin - Units
Description

Chemistry, Clinical, Bilirubin, total measurement, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201913
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
Total Bilirubin - Low
Description

Chemistry, Clinical, Bilirubin, total measurement, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201913
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
Total Bilirubin - High
Description

Chemistry, Clinical, Bilirubin, total measurement, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201913
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
Total Bilirubin - Tox Grade
Description

Chemistry, Clinical, Bilirubin, total measurement, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201913
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
Carbon Dioxide
Description

Chemistry, Clinical, Carbon Dioxide

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0007012
Carbon Dioxide - Result
Description

Chemistry, Clinical, Carbon Dioxide, Result

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0007012
UMLS CUI [1,3]
C1274040
Carbon Dioxide - Units
Description

Chemistry, Clinical, Carbon Dioxide, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0007012
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
Carbon Dioxide - Low
Description

Chemistry, Clinical, Carbon Dioxide, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0007012
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
Carbon Dioxide - High
Description

Chemistry, Clinical, Carbon Dioxide, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0007012
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
Carbon Dioxide - Tox Grade
Description

Chemistry, Clinical, Carbon Dioxide, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0007012
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
BUN
Description

Chemistry, Clinical, Blood urea nitrogen measurement

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0005845
BUN - Result
Description

Chemistry, Clinical, Blood urea nitrogen measurement, Result

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0005845
UMLS CUI [1,3]
C1274040
BUN - Units
Description

Chemistry, Clinical, Blood urea nitrogen measurement, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0005845
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
BUN - Low
Description

Chemistry, Clinical, Blood urea nitrogen measurement, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0005845
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
BUN - High
Description

Chemistry, Clinical, Blood urea nitrogen measurement, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0005845
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
BUN - Tox Grade
Description

Chemistry, Clinical, Blood urea nitrogen measurement, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0005845
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
Calcium
Description

Chemistry, Clinical, Calcium measurement

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201925
Calcium - Result
Description

Chemistry, Clinical, Calcium measurement, Result

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201925
UMLS CUI [1,3]
C1274040
Calcium - Units
Description

Chemistry, Clinical, Calcium measurement, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201925
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
Calcium - Low
Description

Chemistry, Clinical, Calcium measurement, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201925
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
Calcium - High
Description

Chemistry, Clinical, Calcium measurement, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201925
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
Calcium - Tox Grade
Description

Chemistry, Clinical, Calcium measurement, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201925
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
Creatinine
Description

Chemistry, Clinical, Creatinine measurement

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201975
Creatinine - Result
Description

Chemistry, Clinical, Creatinine measurement, Result

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201975
UMLS CUI [1,3]
C1274040
Creatinine - Units
Description

Chemistry, Clinical, Creatinine measurement, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201975
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
Creatinine - Low
Description

Chemistry, Clinical, Creatinine measurement, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201975
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
Creatinine - High
Description

Chemistry, Clinical, Creatinine measurement, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201975
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
Creatinine - Tox Grade
Description

Chemistry, Clinical, Creatinine measurement, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201975
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
Magnesium
Description

Chemistry, Clinical, Magnesium measurement

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0373675
Magnesium - Result
Description

Chemistry, Clinical, Magnesium measurement, Result

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0373675
UMLS CUI [1,3]
C1274040
Magnesium - Units
Description

Chemistry, Clinical, Magnesium measurement, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0373675
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
Magnesium - Low
Description

Chemistry, Clinical, Magnesium measurement, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0373675
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
Magnesium - High
Description

Chemistry, Clinical, Magnesium measurement, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0373675
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
Magnesium - Tox Grade
Description

Chemistry, Clinical, Magnesium measurement, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0373675
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
Potassium
Description

Chemistry, Clinical, Potassium measurement

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0202194
Potassium - Result
Description

Chemistry, Clinical, Potassium measurement, Result

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0202194
UMLS CUI [1,3]
C1274040
Potassium - Units
Description

Chemistry, Clinical, Potassium measurement, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0202194
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
Potassium - Low
Description

Chemistry, Clinical, Potassium measurement, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0202194
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
Potassium - High
Description

Chemistry, Clinical, Potassium measurement, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0202194
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
Potassium - Tox Grade
Description

Chemistry, Clinical, Potassium measurement, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0202194
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
Sodium
Description

Chemistry, Clinical, Sodium measurement

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0337443
Sodium - Result
Description

Chemistry, Clinical, Sodium measurement, Result

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0337443
UMLS CUI [1,3]
C1274040
Sodium - Units
Description

Chemistry, Clinical, Sodium measurement, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0337443
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
Sodium - Low
Description

Chemistry, Clinical, Sodium measurement, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0337443
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
Sodium - High
Description

Chemistry, Clinical, Sodium measurement, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0337443
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
Sodium - Tox Grade
Description

Chemistry, Clinical, Sodium measurement, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0337443
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
H. pylori serology (IgG)
Description

Chemistry, Clinical, Helicobacter pylori

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0079488
H. pylori serology (IgG) - Result
Description

Chemistry, Clinical, Helicobacter pylori, Result

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0079488
UMLS CUI [1,3]
C1274040
H. pylori serology (IgG) - Units
Description

Chemistry, Clinical, Helicobacter pylori, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0079488
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
H. pylori serology (IgG) - Low
Description

Chemistry, Clinical, Helicobacter pylori, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0079488
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
H. pylori serology (IgG) - High
Description

Chemistry, Clinical, Helicobacter pylori, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0079488
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
H. pylori serology (IgG) - Tox Grade
Description

Chemistry, Clinical, Helicobacter pylori, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0079488
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
Creatinine Clearance
Description

Chemistry, Clinical, Creatinine clearance measurement

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0373595
Creatinine Clearance - Result
Description

Chemistry, Clinical, Creatinine clearance measurement, Result

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0373595
UMLS CUI [1,3]
C1274040
Creatinine Clearance - Units
Description

Chemistry, Clinical, Creatinine clearance measurement, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0373595
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
Creatinine Clearance - Low
Description

Chemistry, Clinical, Creatinine clearance measurement, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0373595
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
Creatinine Clearance - High
Description

Chemistry, Clinical, Creatinine clearance measurement, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0373595
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
Creatinine Clearance - Tox Grade
Description

Chemistry, Clinical, Creatinine clearance measurement, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0373595
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
Was any test on this page performed at a different lab than specified on this page?
Description

Laboratory Procedures, Chemistry, Clinical, Laboratory, Other

Data type

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0008000
UMLS CUI [1,3]
C0022877
UMLS CUI [1,4]
C0205394
Local Laboratory - Haematology
Description

Local Laboratory - Haematology

Alias
UMLS CUI-1
C0022885
UMLS CUI-2
C0474523
Laboratory Used For This Sample
Description

Laboratory, Hematology finding

Data type

text

Alias
UMLS CUI [1,1]
C0022877
UMLS CUI [1,2]
C0474523
Gender used to determine lab normals
Description

Laboratory Procedures, Hematology finding, Gender

Data type

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0474523
UMLS CUI [1,3]
C0079399
Date of birth used to determine lab normals
Description

Laboratory Procedures, Hematology finding, Patient date of birth

Data type

date

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0474523
UMLS CUI [1,3]
C0421451
Date sample taken
Description

Laboratory Procedures, Hematology finding, Sampling, Date in time

Data type

date

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0474523
UMLS CUI [1,3]
C0870078
UMLS CUI [1,4]
C0011008
RBC
Description

Hematology finding, Red Blood Cell Count measurement

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0014772
RBC - Result
Description

Hematology finding, Red Blood Cell Count measurement, Result

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0014772
UMLS CUI [1,3]
C1274040
RBC - Units
Description

Hematology finding, Red Blood Cell Count measurement, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0014772
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
RBC - Low
Description

Hematology finding, Red Blood Cell Count measurement, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0014772
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
RBC - High
Description

Hematology finding, Red Blood Cell Count measurement, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0014772
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
RBC - Tox Grade
Description

Hematology finding, Red Blood Cell Count measurement, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0014772
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
Haemoglobin
Description

Hematology finding, Hemoglobin

Data type

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0474523
Haemoglobin - Result
Description

Hematology finding, Hemoglobin, Result

Data type

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0474523
UMLS CUI [1,3]
C1274040
Haemoglobin - Units
Description

Hematology finding, Hemoglobin, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0474523
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
Haemoglobin - Low
Description

Hematology finding, Hemoglobin, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0474523
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
Haemoglobin - High
Description

Hematology finding, Hemoglobin, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0474523
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
Haemoglobin - Tox Grade
Description

Hematology finding, Hemoglobin, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0474523
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
Haematocrit
Description

Hematology finding, Hematocrit level

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0518014
Haematocrit - Result
Description

Hematology finding, Hematocrit level, Result

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0518014
UMLS CUI [1,3]
C1274040
Haematocrit - Units
Description

Hematology finding, Hematocrit level, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0518014
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
Haematocrit - Low
Description

Hematology finding, Hematocrit level, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0518014
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
Haematocrit - High
Description

Hematology finding, Hematocrit level, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0518014
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
Haematocrit - Tox Grade
Description

Hematology finding, Hematocrit level, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0518014
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
Platelets
Description

Hematology finding, Blood Platelets

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0005821
Platelets - Result
Description

Hematology finding, Blood Platelets, Result

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0005821
UMLS CUI [1,3]
C1274040
Platelets - Units
Description

Hematology finding, Blood Platelets, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0005821
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
Platelets - Low
Description

Hematology finding, Blood Platelets, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0005821
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
Platelets - High
Description

Hematology finding, Blood Platelets, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0005821
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
Platelets - Tox Grade
Description

Hematology finding, Blood Platelets, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0005821
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
WBC
Description

Hematology finding, White Blood Cell Count procedure

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0023508
WBC - Result
Description

Hematology finding, White Blood Cell Count procedure, Result

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0023508
UMLS CUI [1,3]
C1274040
WBC - Units
Description

Hematology finding, White Blood Cell Count procedure, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0023508
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
WBC - Low
Description

Hematology finding, White Blood Cell Count procedure, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0023508
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
WBC - High
Description

Hematology finding, White Blood Cell Count procedure, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0023508
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
WBC - Tox Grade
Description

Hematology finding, White Blood Cell Count procedure, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0023508
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
Differential Units
Description

Hematology finding, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C1519795
Basophils
Description

Hematology finding, Blood basophil count (lab test)

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200641
Basophils - Result
Description

Hematology finding, Blood basophil count (lab test), Result

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200641
UMLS CUI [1,3]
C1274040
Basophils - Units
Description

Hematology finding, Blood basophil count (lab test), Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200641
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
Basophils - Low
Description

Hematology finding, Blood basophil count (lab test), Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200641
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
Basophils - High
Description

Hematology finding, Blood basophil count (lab test), Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200641
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
Basophils - Tox Grade
Description

Hematology finding, Blood basophil count (lab test), Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200641
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
Eosinophils
Description

Hematology finding, Eosinophil count procedure

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200638
Eosinophils - Result
Description

Hematology finding, Eosinophil count procedure, Result

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200638
UMLS CUI [1,3]
C1274040
Eosinophils - Units
Description

Hematology finding, Eosinophil count procedure, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200638
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
Eosinophils - Low
Description

Hematology finding, Eosinophil count procedure, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200638
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
Eosinophils - High
Description

Hematology finding, Eosinophil count procedure, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200638
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
Eosinophils - Tox Grade
Description

Hematology finding, Eosinophil count procedure, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200638
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
Lymphocytes
Description

Hematology finding, Lymphocyte Count measurement

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200635
Lymphocytes - Result
Description

Hematology finding, Lymphocyte Count measurement, Result

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200635
UMLS CUI [1,3]
C1274040
Lymphocytes - Units
Description

Hematology finding, Lymphocyte Count measurement, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200635
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
Lymphocytes - Low
Description

Hematology finding, Lymphocyte Count measurement, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200635
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
Lymphocytes - High
Description

Hematology finding, Lymphocyte Count measurement, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200635
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
Lymphocytes - Tox Grade
Description

Hematology finding, Lymphocyte Count measurement, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200635
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
Monocytes
Description

Hematology finding, Monocyte count result

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0750880
Monocytes - Result
Description

Hematology finding, Monocyte count result, Result

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0750880
UMLS CUI [1,3]
C1274040
Monocytes - Units
Description

Hematology finding, Monocyte count result, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0750880
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
Monocytes - Low
Description

Hematology finding, Monocyte count result, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0750880
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
Monocytes - High
Description

Hematology finding, Monocyte count result, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0750880
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
Monocytes - Tox Grade
Description

Hematology finding, Monocyte count result, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0750880
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
Neutrophils
Description

Hematology finding, Absolute neutrophil count

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0948762
Neutrophils - Result
Description

Hematology finding, Absolute neutrophil count, Result

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0948762
UMLS CUI [1,3]
C1274040
Neutrophils - Units
Description

Hematology finding, Absolute neutrophil count, Result, Unit of Measure

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0948762
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519795
Neutrophils - Low
Description

Hematology finding, Absolute neutrophil count, Result, Lower limit of reference range

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0948762
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1272773
Neutrophils - High
Description

Hematology finding, Absolute neutrophil count, Result, Upper Limit of Normal

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0948762
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C1519815
Neutrophils - Tox Grade
Description

Hematology finding, Absolute neutrophil count, Result, Toxicity Grade

Data type

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0948762
UMLS CUI [1,3]
C1274040
UMLS CUI [1,4]
C2826262
Was any test on this page performed at a different lab than specified on this page?
Description

Laboratory Procedures, Hematology finding, Laboratory, Other

Data type

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0474523
UMLS CUI [1,3]
C0022877
UMLS CUI [1,4]
C0205394
Subject Identification
Description

Subject Identification

Alias
UMLS CUI-1
C2348585
Subject number
Description

Clinical Trial Subject Unique Identifier

Data type

integer

Alias
UMLS CUI [1]
C2348585
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Similar models

Screen

1 forms
  1. StudyEvent: ODM
    1. Screen
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Inform Screening
C0220908 (UMLS CUI-1)
Clinical trial participant (person), Person Initials
Item
Subject initials
text
C1997894 (UMLS CUI [1,1])
C2986440 (UMLS CUI [1,2])
Patient date of birth
Item
Date of birth
date
C0421451 (UMLS CUI [1])
Item Group
Inform Enrollment
C1516879 (UMLS CUI-1)
Clinical Trial Subject Unique Identifier
Item
Subject number
text
C2348585 (UMLS CUI [1])
Item Group
Date of Visit
C1320303 (UMLS CUI-1)
Date of visit, Assessment Date
Item
Date of visit/assessment
date
C1320303 (UMLS CUI [1,1])
C2985720 (UMLS CUI [1,2])
Item Group
Demography
C0011298 (UMLS CUI-1)
Patient date of birth
Item
Date of birth
date
C0421451 (UMLS CUI [1])
Item
Sex
text
C0079399 (UMLS CUI [1])
Gender
Code List
Sex
CL Item
Male (1)
Item
Ethnicity
text
C0015031 (UMLS CUI [1])
Ethnic group
Code List
Ethnicity
CL Item
Hispanic or Latino (1)
CL Item
Not Hispanic or Latino (2)
Item
Geographic ancestry
text
C3841890 (UMLS CUI [1])
Your ancestry or national origin
Code List
Geographic ancestry
CL Item
African American/African Heritage (1)
CL Item
American Indian or Alaskan Native (2)
CL Item
Asian - Central/South Asian Heritage (3)
CL Item
Asian - East Asian Heritage (4)
CL Item
Asian - Japanese Heritage (5)
CL Item
Asian - South East Asian Heritage (6)
CL Item
Native Hawaiian or Other Pacific Islander  (7)
CL Item
White - Arabic/North African Heritage (8)
CL Item
White - White/Caucasian/European Heritage (9)
Item Group
Eligibility Question
C0013893 (UMLS CUI-1)
Eligibility Determination
Item
Did the subject meet all the entry criteria?
boolean
C0013893 (UMLS CUI [1])
Item Group
Inclusion Criteria
C1512693 (UMLS CUI-1)
Breast Carcinoma, Metastatic to, Estrogen receptor positive breast cancer; Malignant Neoplasms, Unresponsive to Treatment
Item
Histologically or cytologically confirmed diagnosis of: • Metastatic breast cancer that overexpresses ErbB2 (3+ by IHC, FISH, or CISH positive) OR • Recurrent, advanced, or metastatic solid tumor malignancy that is refractory to standard therapies, for which there is no approved therapy, and for which lapatinib in combination with one of the permitted anti-cancer regimens in the companion rollover protocol (EGF111767) may be suitable.
boolean
C0678222 (UMLS CUI [1,1])
C0036525 (UMLS CUI [1,2])
C2938924 (UMLS CUI [1,3])
C0006826 (UMLS CUI [2,1])
C0205269 (UMLS CUI [2,2])
Age
Item
Is at least 18 years of age and not greater than 75 years of age.
boolean
C0001779 (UMLS CUI [1])
Gender
Item
Is male or female.
boolean
C0079399 (UMLS CUI [1])
Childbearing Potential
Item
A female is eligible to enter and participate in the study if she is of: a. Non-childbearing potential (i.e. physiologically incapable of becoming pregnant), including any female who: • Has had a hysterectomy • Has had a bilateral oophorectomy (ovariectomy) • Has had a bilateral tubal ligation, or • Is post-menopausal (a demonstration of total cessation of menses for ≥ 1 year) or b. Childbearing potential, has a negative serum pregnancy test at Screening and agrees to one of the following:• Double-barrier contraception (condom with spermicidal jelly, foam, suppository, or film; diaphragm with spermicide; or male condom and diaphragm). • Complete abstinence from sexual intercourse from two weeks prior to administration of the study drug, throughout the active study treatment period, and two weeks post last administration of the study drug. • Vasectomized partner who is sterile prior to the female subject’s entry and is the sole sexual partner for that female.
boolean
C3831118 (UMLS CUI [1])
Oral medication, Able to swallow; Oral medication, Ability, Retained
Item
Is able to swallow and retain oral medication.
boolean
C0175795 (UMLS CUI [1,1])
C2712086 (UMLS CUI [1,2])
C0175795 (UMLS CUI [2,1])
C0085732 (UMLS CUI [2,2])
C0333118 (UMLS CUI [2,3])
ECOG Performance status
Item
ECOG performance status 0 to 2.
boolean
C1520224 (UMLS CUI [1])
Bone Marrow, physiological aspects
Item
Adequate bone marrow function. • Hemoglobin ≥ 9 gm/dL (90g/L). • Absolute granulocyte count ≥ 1,500/mm3 (1.5 x 109/L). • Platelets ≥ 75,000/mm3 (75 x 109/L).
boolean
C0005953 (UMLS CUI [1,1])
C0031843 (UMLS CUI [1,2])
Estimation of creatinine clearance by Cockcroft-Gault formula
Item
Calculated creatinine clearance (CrCl) ≥ 50 ml/min based on Cockcroft and Gault
boolean
C2711451 (UMLS CUI [1])
Bilirubin, total measurement
Item
Total bilirubin ≤ 1.5 X upper limit of normal of institutional values.
boolean
C0201913 (UMLS CUI [1])
Alanine aminotransferase measurement
Item
Alanine transaminase (ALT) ≤ 3 times the upper limit of the institutional values or ≤ 5 times ULN with documented liver metastases
boolean
C0201836 (UMLS CUI [1])
Left ventricular ejection fraction
Item
Has a left ventricular ejection fraction (LVEF) within the normal institutional range based on ECHO or MUGA.
boolean
C0428772 (UMLS CUI [1])
Life Expectancy
Item
Life expectancy of ≥ 12 weeks
boolean
C0023671 (UMLS CUI [1])
Informed Consent
Item
Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
boolean
C0021430 (UMLS CUI [1])
Item Group
Exclusion Criteria
C0680251 (UMLS CUI-1)
Pregnancy; Breast Feeding
Item
Is pregnant or lactating.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Malabsorption Syndrome; Disease, Affecting, gastrointestinal function; Colon resection; Stomach, Excision; Small intestine excision
Item
Has malabsorption syndrome, a disease affecting gastrointestinal function, or resection of the colon, stomach or small bowel.
boolean
C0024523 (UMLS CUI [1])
C0012634 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C0516983 (UMLS CUI [2,3])
C4069040 (UMLS CUI [3])
C0161898 (UMLS CUI [4,1])
C0728940 (UMLS CUI [4,2])
C0192601 (UMLS CUI [5])
Liver diseases; Biliary System Disorder
Item
Has current active hepatic or biliary disease (with exception of patients with Gilbert's syndrome, asymptomatic gallstones, liver metastases or stable chronic liver disease per investigator assessment)
boolean
C0023895 (UMLS CUI [1])
C3275124 (UMLS CUI [2])
Metastatic malignant neoplasm to brain; Leptomeningeal Neoplasms
Item
Has evidence of symptomatic or uncontrolled brain metastases or leptomeningeal disease. Subjects with brain metastases treated by surgery and/or radiotherapy are eligible if neurologically stable and do not require steroids or anticonvulsants for at least 28 days prior to the first dose of study drug.
boolean
C0220650 (UMLS CUI [1])
C0751297 (UMLS CUI [2])
Medically unfit, Clinical Trials
Item
Is considered medically unfit for the study by the investigator as a result of the medical interview, physical exam, or screening investigations.
boolean
C3841806 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
Benzimidazole derivatives, antinematodal, Hypersensitivity; Experimental drug, Idiosyncrasy
Item
Has a known immediate or delayed benzimidazole hypersensitivity reaction or idiosyncrasy to drugs chemically related to the investigational product such as gefitinib [Iressa] and erlotinib [Tarceva].
boolean
C3653457 (UMLS CUI [1,1])
C0020517 (UMLS CUI [1,2])
C0304229 (UMLS CUI [2,1])
C0231191 (UMLS CUI [2,2])
Esomeprazole, Hypersensitivity
Item
Has a known hypersensitivity to esomeprazole.
boolean
C0937846 (UMLS CUI [1,1])
C0020517 (UMLS CUI [1,2])
Experimental drug, Previous
Item
Has received treatment with any investigational drug in the previous four weeks. (with the exception of lapatinib).
boolean
C0304229 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
Chemotherapy Regimen, Cancer treatment, Previous; Immunotherapy, Cancer treatment, Previous; Biological treatment, Cancer treatment, Previous; Hormone Therapy, Cancer treatment, Previous
Item
Has received chemotherapy, immunotherapy, biologic therapy or hormonal therapy for the treatment of cancer within the past 14 days, with the exception of mitomycin C which is restricted for the past six weeks, and lapatinib. Subjects receiving lapatinib prior to study entry are eligible to participate in the study. NOTE: Any ongoing potentially reversible toxicity from prior anti-cancer therapy that is > Grade 1 or any toxicity from prior anti-cancer therapy that is progressing in severity will render the subject ineligible.
boolean
C0392920 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C0205156 (UMLS CUI [1,3])
C0021083 (UMLS CUI [2,1])
C0920425 (UMLS CUI [2,2])
C0205156 (UMLS CUI [2,3])
C1531518 (UMLS CUI [3,1])
C0920425 (UMLS CUI [3,2])
C0205156 (UMLS CUI [3,3])
C0279025 (UMLS CUI [4,1])
C0920425 (UMLS CUI [4,2])
C0205156 (UMLS CUI [4,3])
Pharmaceutical Preparations, prohibition
Item
Is receiving any prohibited medication within the timeframe indicated on the prohibited medication list
boolean
C0013227 (UMLS CUI [1,1])
C0683610 (UMLS CUI [1,2])
Protocol compliance, Unpermitted
Item
Has physiological, familial, sociological, or geographical conditions that do not permit compliance with the protocol.
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
venous access, Inadequate (qualifier)
Item
Has inadequate venous access for protocol-related blood draws.
boolean
C0750164 (UMLS CUI [1,1])
C0205412 (UMLS CUI [1,2])
ECG abnormality
Item
Clinically significant electrocardiogram (ECG) abnormality including baseline QTc prolongation >480msec, 2nd degree (type II), or 3rd degree AV block.
boolean
C1832603 (UMLS CUI [1])
Heparin, Hypersensitivity; Heparin-induced Thrombocytopenia
Item
History of sensitivity to heparin or heparin-induced thrombocytopenia.
boolean
C0019134 (UMLS CUI [1,1])
C0020517 (UMLS CUI [1,2])
C0272285 (UMLS CUI [2])
Red wine; Citrus aurantium; Grapefruit (food); GRAPEFRUIT JUICE
Item
Consumption of red wine, seville oranges, grapefruit or grapefruit juice and/or kumquats, pummelos, exotic citrus fruit (i.e. star fruit, bitter melon), grapefruit hybrids or fruit juices from seven days prior to the first dose of study medication.
boolean
C0349371 (UMLS CUI [1])
C0330922 (UMLS CUI [2])
C0995150 (UMLS CUI [3])
C0452456 (UMLS CUI [4])
Item Group
ECHO/MUGA
C0013516 (UMLS CUI-1)
C0521317 (UMLS CUI-2)
Item
Scan Type
text
C0013516 (UMLS CUI [1])
C0521317 (UMLS CUI [2])
Echocardiography; Multiple gated acquisition scanning
Code List
Scan Type
CL Item
ECHO (1)
CL Item
MUGA (2)
Echocardiography, Date in time, Time; Multiple gated acquisition scanning, Date in time, Time
Item
Date and time of scan
datetime
C0013516 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
C0521317 (UMLS CUI [2,1])
C0011008 (UMLS CUI [2,2])
C0040223 (UMLS CUI [2,3])
Left ventricular ejection fraction
Item
Left ventricular ejection fraction (LVEF)
integer
C0428772 (UMLS CUI [1])
Item
Scan results
text
C0013516 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
C0521317 (UMLS CUI [2,1])
C1274040 (UMLS CUI [2,2])
Echocardiography, Result; Multiple gated acquisition scanning, Result
Code List
Scan results
CL Item
Normal (1)
CL Item
Abnormal, describe abnormality (2)
Item
Describe abnormality
text
C0013516 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
C0521317 (UMLS CUI [2,1])
C1274040 (UMLS CUI [2,2])
Echocardiography, Result; Multiple gated acquisition scanning, Result
Code List
Describe abnormality
Item Group
Medical Conditions
C0012634 (UMLS CUI-1)
Disease
Item
Does the subject have any current or past cancer or non-cancer related medical conditions?
boolean
C0012634 (UMLS CUI [1])
Disease, Sequence Number
Item
Sequence Number
integer
C0012634 (UMLS CUI [1,1])
C2348184 (UMLS CUI [1,2])
Disease
Item
Specific Condition
text
C0012634 (UMLS CUI [1])
Item
Modified Term
text
C0012634 (UMLS CUI [1,1])
C2826302 (UMLS CUI [1,2])
Ophthalmic examination and evaluation, Color Assessment, Right eye
Code List
Modified Term
Disease, Medical Dictionary for Regulatory Activities Terminology (MedDRA), Synonym
Item
MedDRA Synonym
text
C0012634 (UMLS CUI [1,1])
C1140263 (UMLS CUI [1,2])
C0871468 (UMLS CUI [1,3])
Item
MedDRA lower level term code
text
C0012634 (UMLS CUI [1,1])
C3898442 (UMLS CUI [1,2])
Ophthalmic examination and evaluation, Color Assessment, Right eye
Code List
MedDRA lower level term code
Disease, Code, Failed
Item
Failed coding
text
C0012634 (UMLS CUI [1,1])
C0805701 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
Item
Status
text
C0012634 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
Ophthalmic examination and evaluation, Color Assessment, Right eye
Code List
Status
CL Item
Current (1)
CL Item
Past (2)
Item Group
Disease Characteristics
C0599878 (UMLS CUI-1)
Item
Tumour Classification at Initial Diagnosis
text
C0677930 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
C4071762 (UMLS CUI [1,3])
primary tumor, Type - attribute, at initial diagnosis
Code List
Tumour Classification at Initial Diagnosis
CL Item
Cutaneous (1)
CL Item
Non-cutaneous (2)
CL Item
Inflammatory (3)
CL Item
Unknown (4)
CL Item
Other, specify (5)
Malignant Neoplasms, Diagnosis, Date in time
Item
Date of Initial Diagnosis
date
C0006826 (UMLS CUI [1,1])
C0011900 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Item
Stage at Initial Diagnosis
text
C0006826 (UMLS CUI [1,1])
C1300072 (UMLS CUI [1,2])
C4071762 (UMLS CUI [1,3])
Malignant Neoplasms, Tumor stage, at initial diagnosis
Code List
Stage at Initial Diagnosis
CL Item
0 (1)
CL Item
Ia (2)
CL Item
Ib (3)
CL Item
Ic (4)
CL Item
IIa (5)
CL Item
IIb (6)
CL Item
IIc (7)
CL Item
IIIa (8)
CL Item
IIIb (9)
CL Item
IIIc (10)
CL Item
IVa (11)
CL Item
IVb (12)
CL Item
IVc (13)
CL Item
Unknown (14)
Item
Histology at Initial Diagnosis
text
C0006826 (UMLS CUI [1,1])
C0019638 (UMLS CUI [1,2])
C4071762 (UMLS CUI [1,3])
Malignant Neoplasms, Histology, at initial diagnosis
Code List
Histology at Initial Diagnosis
CL Item
Adenocarcinoma (1)
CL Item
Infiltrating ductal NOS (2)
CL Item
Lobular invasive (3)
CL Item
Malignant mucinous tumours (4)
CL Item
Squamous (5)
CL Item
Undifferentiated adenocarcinoma (6)
CL Item
Undifferentiated carcinoma (7)
CL Item
Tubular (8)
CL Item
Unknown (9)
CL Item
Other, specify (10)
Item
Other, specify
text
C0006826 (UMLS CUI [1,1])
C0019638 (UMLS CUI [1,2])
C4071762 (UMLS CUI [1,3])
Malignant Neoplasms, Histology, at initial diagnosis
Code List
Other, specify
Item
ErbB2 (Her2/neu) Status ImmunoHisto-Chemistry (IHC)
text
C0006826 (UMLS CUI [1,1])
C1512413 (UMLS CUI [1,2])
C0021044 (UMLS CUI [1,3])
Malignant Neoplasms, HER2/Neu Status, Immunohistochemistry
Code List
ErbB2 (Her2/neu) Status ImmunoHisto-Chemistry (IHC)
CL Item
1+ (1)
CL Item
2+ (2)
CL Item
3+ (3)
Item
Fluorescence in situ Hybridization (FISH)
text
C0006826 (UMLS CUI [1,1])
C0162789 (UMLS CUI [1,2])
Malignant Neoplasms, Fluorescent in Situ Hybridization
Code List
Fluorescence in situ Hybridization (FISH)
CL Item
Positive (1)
CL Item
Negative (2)
Neoplasm Metastatis, Date of Diagnosis
Item
Date Metastatic Disease was First Diagnosed
date
C0027627 (UMLS CUI [1,1])
C2316983 (UMLS CUI [1,2])
Item
Abdomen/Abdominal Wall
text
C0027627 (UMLS CUI [1,1])
C0000726 (UMLS CUI [1,2])
C0027627 (UMLS CUI [2,1])
C0836916 (UMLS CUI [2,2])
Neoplasm Metastasis, Abdomen, Abdominal wall structure
Code List
Abdomen/Abdominal Wall
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Adrenals
text
C0027627 (UMLS CUI [1,1])
C0001625 (UMLS CUI [1,2])
Neoplasm Metastasis, Abdomen, Abdominal wall structure
Code List
Adrenals
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Bladder
text
C0027627 (UMLS CUI [1,1])
C0005682 (UMLS CUI [1,2])
Neoplasm Metastasis, Abdomen, Abdominal wall structure
Code List
Bladder
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Blood
text
C0027627 (UMLS CUI [1,1])
C0005767 (UMLS CUI [1,2])
Neoplasm Metastasis, Abdomen, Abdominal wall structure
Code List
Blood
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Bone
text
C0027627 (UMLS CUI [1,1])
C0262950 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Bone
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Bone Marrow
text
C0027627 (UMLS CUI [1,1])
C0005953 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Bone Marrow
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Breast
text
C0027627 (UMLS CUI [1,1])
C0006141 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Breast
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Cervix
text
C0027627 (UMLS CUI [1,1])
C0007874 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Cervix
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Chest Wall
text
C0027627 (UMLS CUI [1,1])
C0205076 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Chest Wall
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
CNS
text
C0027627 (UMLS CUI [1,1])
C0686377 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
CNS
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Colon
text
C0027627 (UMLS CUI [1,1])
C0009368 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Colon
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Esophagus/Oesophagus
text
C0027627 (UMLS CUI [1,1])
C0014876 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Esophagus/Oesophagus
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Head and Neck
text
C0027627 (UMLS CUI [1,1])
C0460004 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Head and Neck
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Heart
text
C0027627 (UMLS CUI [1,1])
C0018787 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Heart
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Kidney
text
C0027627 (UMLS CUI [1,1])
C0022646 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Kidney
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Liver
text
C0027627 (UMLS CUI [1,1])
C0023884 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Liver
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Lung
text
C0027627 (UMLS CUI [1,1])
C0024109 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Lung
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Lymph Nodes
text
C0027627 (UMLS CUI [1,1])
C0024204 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Lymph Nodes
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Oral cavity
text
C0027627 (UMLS CUI [1,1])
C0226896 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Oral cavity
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Ovary
text
C0027627 (UMLS CUI [1,1])
C0029939 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Ovary
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Pancreas
text
C0027627 (UMLS CUI [1,1])
C0030274 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Pancreas
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Peritoneum
text
C0027627 (UMLS CUI [1,1])
C0031153 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Peritoneum
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Pleura
text
C0027627 (UMLS CUI [1,1])
C0032225 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Pleura
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Rectum
text
C0027627 (UMLS CUI [1,1])
C0034896 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Rectum
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Skin
text
C0027627 (UMLS CUI [1,1])
C1123023 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Skin
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Small Intestine
text
C0027627 (UMLS CUI [1,1])
C0021852 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Small Intestine
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Spleen
text
C0027627 (UMLS CUI [1,1])
C0037993 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Spleen
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Stomach
text
C0027627 (UMLS CUI [1,1])
C0038351 (UMLS CUI [1,2])
Neoplasm Metastasis, Skeletal bone
Code List
Stomach
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Thyroid
text
C0027627 (UMLS CUI [1,1])
C0040132 (UMLS CUI [1,2])
Neoplasm Metastasis, Thyroid Gland
Code List
Thyroid
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Other
text
C0027627 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Neoplasm Metastasis, Other
Code List
Other
CL Item
Not Assessed (1)
CL Item
No (2)
CL Item
Yes, please specify (3)
Neoplasm Metastasis, Other
Item
Please specify
text
C0027627 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Item Group
Prior Anti-Cancer Therapy
C0920425 (UMLS CUI-1)
C1514463 (UMLS CUI-2)
Cancer treatment, Prior Therapy
Item
Has the subject taken any prior cancer related therapy?
boolean
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
Cancer treatment, Prior Therapy, Sequence Number
Item
Sequence Number
integer
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,3])
Cancer treatment, Prior Therapy, Medication name
Item
Drug Name
integer
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,3])
Cancer treatment, Prior Therapy, Reported term
Item
Modified reported term
text
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C2826302 (UMLS CUI [1,3])
Cancer treatment, Prior Therapy, Synonym
Item
GSK Drug synonym
text
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C0871468 (UMLS CUI [1,3])
Cancer treatment, Prior Therapy, Collection, Code
Item
GSK Drug Collection code
text
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C1516698 (UMLS CUI [1,3])
C0805701 (UMLS CUI [1,4])
Cancer treatment, Prior Therapy, Code, Failed
Item
Failed coding
text
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])
C0231175 (UMLS CUI [1,4])
Item
Therapy Type
text
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C0920425 (UMLS CUI [1,3])
Cancer treatment, Prior Therapy, Type
Code List
Therapy Type
CL Item
Biologic Therapy (antibodies, cytokines, vaccines) (1)
CL Item
Chemotherapy (cytotoxics, non-cytotoxics) (2)
CL Item
Hormonal Therapy (3)
CL Item
Immunotherapy (4)
Item
Number of Cycles
integer
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C1511572 (UMLS CUI [1,3])
C0237753 (UMLS CUI [1,4])
Cancer treatment, Prior Therapy, Type
Code List
Number of Cycles
Item
Intent
text
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C1283828 (UMLS CUI [1,3])
Cancer treatment, Prior Therapy, Type
Code List
Intent
CL Item
Neo-adjuvant (1)
CL Item
Adjuvant (2)
CL Item
Advanced or Metastatic (3)
CL Item
Local/Regional (4)
CL Item
Prophylactic (5)
CL Item
Radiosensitizer (6)
CL Item
Maintenance (7)
CL Item
ot Applicable  (8)
Cancer treatment, Prior Therapy, Start Date
Item
Start Date
date
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
Cancer treatment, Prior Therapy, End Date
Item
Stop Date
date
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
Item
Best Response
text
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C2986560 (UMLS CUI [1,3])
Cancer treatment, Prior Therapy, Best Overall Response
Code List
Best Response
CL Item
Complete Response (1)
CL Item
Partial Response (2)
CL Item
Stable Disease (3)
CL Item
Progressive Disease (4)
CL Item
Unknown (5)
CL Item
Not Applicable (6)
Item
Cancer therapy treatment
text
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
Cancer treatment, Prior Therapy, Best Overall Response
Code List
Cancer therapy treatment
CL Item
Prior Treatment (1)
CL Item
On-Treatment (2)
CL Item
Post-Treatment (3)
Item Group
Anti-Cancer Radiotherapy
C1522449 (UMLS CUI-1)
C0920425 (UMLS CUI-2)
Therapeutic radiology procedure, cancer treatment
Item
Has the subject received any prior anti-cancer radiotherapy?
boolean
C1522449 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
Therapeutic radiology procedure, cancer treatment, Sequence Number
Item
Sequence Number
integer
C1522449 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,3])
Therapeutic radiology procedure, cancer treatment, Anatomic Site
Item
Site
text
C1522449 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C1515974 (UMLS CUI [1,3])
Therapeutic radiology procedure, cancer treatment, Cumulative Dose
Item
Cumulative Dose
text
C1522449 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C2986497 (UMLS CUI [1,3])
Item
Units
text
C1522449 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,3])
Therapeutic radiology procedure, cancer treatment, Unit of Measure
Code List
Units
CL Item
Grays (1)
CL Item
Centigrays (2)
CL Item
x100 Rads (3)
Item
Intent
text
C1522449 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C1283828 (UMLS CUI [1,3])
Therapeutic radiology procedure, cancer treatment, Unit of Measure
Code List
Intent
CL Item
Neo-adjuvant (1)
CL Item
Adjuvant (2)
CL Item
Advanced or Metastatic (3)
CL Item
Local/Regional (4)
CL Item
Prophylactic (5)
CL Item
Other (6)
Therapeutic radiology procedure, cancer treatment, Start Date
Item
Start Date
date
C1522449 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
Therapeutic radiology procedure, cancer treatment, End Date
Item
Stop Date
date
C1522449 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
Item
Best Response
text
C1522449 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C2986560 (UMLS CUI [1,3])
Therapeutic radiology procedure, cancer treatment, Best Overall Response
Code List
Best Response
CL Item
Complete Response (1)
CL Item
Partial Response (2)
CL Item
Stable Disease (3)
CL Item
Progressive Disease (4)
CL Item
Unknown (5)
CL Item
Not Applicable (6)
Item
Cancer therapy treatment
text
C1522449 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
Therapeutic radiology procedure, cancer treatment, Best Overall Response
Code List
Cancer therapy treatment
CL Item
Prior Treatment (1)
CL Item
On Treatment (2)
CL Item
Post Treatment (3)
Item Group
Vital Signs
C0518766 (UMLS CUI-1)
Vital signs, Date in time, Time
Item
Actual date/time
datetime
C0518766 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
Body Height
Item
Height
integer
C0005890 (UMLS CUI [1])
Body Weight
Item
Weight
float
C0005910 (UMLS CUI [1])
Body mass index
Item
BMI
float
C1305855 (UMLS CUI [1])
heart rate while sitting
Item
Sitting heart rate
integer
C2029904 (UMLS CUI [1])
Systolic Pressure, Sitting position
Item
Sitting blood pressure measurement - Systolic
integer
C0871470 (UMLS CUI [1,1])
C0277814 (UMLS CUI [1,2])
Diastolic blood pressure, Sitting position
Item
Sitting blood pressure measurement - Diastolic
integer
C0428883 (UMLS CUI [1,1])
C0277814 (UMLS CUI [1,2])
Item Group
12-Lead ECG
C0430456 (UMLS CUI-1)
12 lead ECG, Date in time, Time
Item
Date and Time of ECG
datetime
C0430456 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
12 lead ECG, Heart rate
Item
Heart rate
integer
C0430456 (UMLS CUI [1,1])
C0018810 (UMLS CUI [1,2])
12 lead ECG, Electrocardiogram: P-R interval
Item
PR Interval
integer
C0430456 (UMLS CUI [1,1])
C0429087 (UMLS CUI [1,2])
12 lead ECG, QRS complex duration
Item
QRS Duration
integer
C0430456 (UMLS CUI [1,1])
C0429025 (UMLS CUI [1,2])
12 lead ECG, QT interval - finding
Item
Uncorrected QT Interval
integer
C0430456 (UMLS CUI [1,1])
C1287082 (UMLS CUI [1,2])
Item
QTc Interval
integer
C0430456 (UMLS CUI [1,1])
C0855331 (UMLS CUI [1,2])
12 lead ECG, Electrocardiogram QT corrected interval, Evaluation Method
Code List
QTc Interval
Item
Result of the ECG
text
C0430456 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
12 lead ECG, Electrocardiogram QT corrected interval, Evaluation Method
Code List
Result of the ECG
CL Item
Normal (1)
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
CL Item
No result (not available) (4)
Item Group
12-Lead ECG Abnormalities
C0430456 (UMLS CUI-1)
C1704258 (UMLS CUI-2)
12 lead ECG, Abnormality, Date in time, Time
Item
Date and Time of ECG
datetime
C0430456 (UMLS CUI [1,1])
C1704258 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
Item
Record clinically significant abnormalities
text
C0430456 (UMLS CUI [1,1])
C1704258 (UMLS CUI [1,2])
12 lead ECG, Abnormality
Code List
Record clinically significant abnormalities
CL Item
No abnormalities (1)
CL Item
Sinus bradycardia (50-59 beats/min) (2)
CL Item
Sinus bradycardia (40-49 beats/min) (3)
CL Item
Sinus bradycardia (30-39 beats/min) (4)
CL Item
Sinus bradycardia (<30 beats/min) (5)
CL Item
Sinus pause (6)
CL Item
Sinus tachycardia (>100 beats/min) (7)
CL Item
Ectopic supraventricular beats (8)
CL Item
Ectopic supraventricular rhythm (9)
CL Item
Wandering atrial pacemaker (10)
CL Item
Multifocal atrial tachycardia (wandering atrial pacemaker w/rate >100 beats/min) (11)
CL Item
Non-sustained supraventricular tachycardia (>100 beats/min, 3-30 beats) (12)
CL Item
Sustained supraventricular tachycardia (>100 beats/min, >30 beats) (13)
CL Item
Atrial flutter (14)
CL Item
Atrial fibrillation (15)
CL Item
Junctional rhythm (<=100 beats/min, defined by narrow QRS complex) (16)
CL Item
Junctional tachycardia (>100 beats/min) (17)
CL Item
Ventricular premature deplorisation (18)
CL Item
Ventricular couplets (19)
CL Item
Bigeminy (20)
CL Item
Trigeminy (21)
CL Item
Electrical alternans (22)
CL Item
R on T phenomenon (23)
CL Item
Ventricular fibrillation (24)
CL Item
Idioventricular rhythm (<=100 beats/min, defined by wide QRS complex) (25)
CL Item
Non-sustained ventricular tachycardia (>100 beats/min, 3-30 beats) (26)
CL Item
Sustained ventricular tachycardia (>100 beats/min, >30 beats) (27)
CL Item
Wide QRS tachycardia (diagnosis unknown (28)
CL Item
Monomorphic non-sustained ventricular tachycardia (>100 beats/min, 3-30 beats) (29)
CL Item
Monomorphic sustained ventricular tachycardia (>100 beats/min, >30 beats) (30)
CL Item
Polymorphic non-sustained ventricular tachycardia (>100 beats/min, 3-30 beats) (31)
CL Item
Polymorphic sustained ventricular tachycardia (>100 beats/min, >30 beats) (32)
CL Item
Torsades de Pointes (TdP) (33)
CL Item
Pacemaker (34)
CL Item
First degree AV block (PR interval >200msec) (35)
CL Item
Short PR Intervak (36)
CL Item
Second degree AV block (Mobitz type 1) (37)
CL Item
Second degree AV block (Mobitz type 2) (38)
CL Item
2:1 AV block (39)
CL Item
Third degree AV block (40)
CL Item
Left axis deviation (QRS axis more negative than -30 degrees) (41)
CL Item
Right axis deviation (QRS axis more positive than +100 degrees) (42)
CL Item
Incomplete left bundle branch block (43)
CL Item
Incomplete left bundle branch block (44)
CL Item
Right bundle branch block (45)
CL Item
Left anterior hemiblock (46)
CL Item
Left posterior hemiblock (47)
CL Item
Left bundle branch block (48)
CL Item
Bifascicular block (49)
CL Item
Non-specific intraventricular conduction delay (QRS >=120 msec) (50)
CL Item
Accessory pathway (Wolff-Parkinson-White, Lown-Ganong-Levine (51)
CL Item
QTc prolongation >=500 msec (52)
CL Item
AV dissociation (53)
CL Item
Myocardial infarction, old (54)
CL Item
Myocardial infarction, non Q-wave (55)
CL Item
Non-specific ST-T changes (56)
CL Item
J point elevation (57)
CL Item
ST elevation (58)
CL Item
ST depression (59)
CL Item
ST segment abnormality (60)
CL Item
U waves (61)
CL Item
T wave inversion (62)
CL Item
T wave peaked (63)
CL Item
T waves biphasic (64)
CL Item
T waves flat (65)
CL Item
66)Notched T-waves (66)Notched T-waves)
CL Item
Low QRS voltage (67)
CL Item
T wave abnormality (68)
CL Item
Other abnormal rhythm (69)
CL Item
Other morphology (70)
CL Item
Other conduction (71)
CL Item
Other myocardial infarction (72)
CL Item
Other depolarization/repolarisation (73)
CL Item
Other abnormality/Cardiologist comments (74)
Item Group
Randomization Number
C0034656 (UMLS CUI-1)
C0237753 (UMLS CUI-2)
Randomisation
Item
Was the subject able to be randomized?
boolean
C0034656 (UMLS CUI [1])
Randomisation, Numbers
Item
Yes, provide Randomization number
integer
C0034656 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
Randomization, Date in time
Item
Yes, provide Date of randomization
date
C0034656 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item Group
Local Laboratory - Clinical Chemistry
C0022885 (UMLS CUI-1)
C0008000 (UMLS CUI-2)
Chemistry, Clinical, Laboratory
Item
Laboratory Used For This Sample
date
C0008000 (UMLS CUI [1,1])
C0022877 (UMLS CUI [1,2])
Chemistry, Clinical, Reference lab test reference range, Gender
Item
Gender used to determine lab normals
text
C0008000 (UMLS CUI [1,1])
C0883335 (UMLS CUI [1,2])
C0079399 (UMLS CUI [1,3])
Chemistry, Clinical, Reference lab test reference range, Patient date of birth
Item
Date of birth used to determine lab normals
date
C0008000 (UMLS CUI [1,1])
C0883335 (UMLS CUI [1,2])
C0421451 (UMLS CUI [1,3])
Chemistry, Clinical, Laboratory
Item
Laboratory Used For This Sample
date
C0008000 (UMLS CUI [1,1])
C0022877 (UMLS CUI [1,2])
Chemistry, Clinical, Sampling, Date in time
Item
Date sample taken
date
C0008000 (UMLS CUI [1,1])
C0870078 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Chemistry, Clinical, Fasting
Item
Was the subject fasting for this laboratory?
boolean
C0008000 (UMLS CUI [1,1])
C0015663 (UMLS CUI [1,2])
Item
Albumin
text
C0008000 (UMLS CUI [1,1])
C0201838 (UMLS CUI [1,2])
Chemistry, Clinical, Albumin measurement
Code List
Albumin
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Albumin measurement, Result
Item
Albumin - Result
text
C0008000 (UMLS CUI [1,1])
C0201838 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Albumin measurement, Result, Unit of Measure
Item
Albumin - Units
text
C0008000 (UMLS CUI [1,1])
C0201838 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Albumin measurement, Result, Lower limit of reference range
Item
Albumin - Low
text
C0008000 (UMLS CUI [1,1])
C0201838 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Albumin measurement, Result, Upper Limit of Normal
Item
Albumin - High
text
C0008000 (UMLS CUI [1,1])
C0201838 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Albumin measurement, Result, Toxicity Grade
Item
Albumin - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0201838 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Alkaline Phosphatase
text
C0008000 (UMLS CUI [1,1])
C0201850 (UMLS CUI [1,2])
Chemistry, Clinical, Alkaline phosphatase measurement
Code List
Alkaline Phosphatase
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Alkaline phosphatase measurement, Result
Item
Alkaline Phosphatase - Result
text
C0008000 (UMLS CUI [1,1])
C0201850 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Alkaline phosphatase measurement, Result, Unit of Measure
Item
Alkaline Phosphatase - Units
text
C0008000 (UMLS CUI [1,1])
C0201850 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Alkaline phosphatase measurement, Result, Lower limit of reference range
Item
Alkaline Phosphatase - Low
text
C0008000 (UMLS CUI [1,1])
C0201850 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Alkaline phosphatase measurement, Result, Upper Limit of Normal
Item
Alkaline Phosphatase - High
text
C0008000 (UMLS CUI [1,1])
C0201850 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Alkaline phosphatase measurement, Result, Toxicity Grade
Item
Alkaline Phosphatase - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0201850 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
ALT
text
C0008000 (UMLS CUI [1,1])
C0201836 (UMLS CUI [1,2])
Chemistry, Clinical, Alanine aminotransferase measurement
Code List
ALT
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Alanine aminotransferase measurement, Result
Item
ALT - Result
text
C0008000 (UMLS CUI [1,1])
C0201836 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Alanine aminotransferase measurement, Result, Unit of Measure
Item
ALT - Units
text
C0008000 (UMLS CUI [1,1])
C0201836 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Alanine aminotransferase measurement, Result, Lower limit of reference range
Item
ALT - Low
text
C0008000 (UMLS CUI [1,1])
C0201836 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Alanine aminotransferase measurement, Result, Upper Limit of Normal
Item
ALT - High
text
C0008000 (UMLS CUI [1,1])
C0201836 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Alanine aminotransferase measurement, Result, Toxicity Grade
Item
ALT - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0201836 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
AST
text
C0008000 (UMLS CUI [1,1])
C0201899 (UMLS CUI [1,2])
Chemistry, Clinical, Aspartate aminotransferase measurement
Code List
AST
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Aspartate aminotransferase measurement, Result
Item
AST - Result
text
C0008000 (UMLS CUI [1,1])
C0201899 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Aspartate aminotransferase measurement, Result, Unit of Measure
Item
AST - Units
text
C0008000 (UMLS CUI [1,1])
C0201899 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Aspartate aminotransferase measurement, Result, Lower limit of reference range
Item
AST - Low
text
C0008000 (UMLS CUI [1,1])
C0201899 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Aspartate aminotransferase measurement, Result, Upper Limit of Normal
Item
AST - High
text
C0008000 (UMLS CUI [1,1])
C0201899 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Aspartate aminotransferase measurement, Result, Toxicity Grade
Item
AST - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0201899 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Direct Bilirubin
text
C0008000 (UMLS CUI [1,1])
C0201916 (UMLS CUI [1,2])
Chemistry, Clinical, Bilirubin, direct measurement
Code List
Direct Bilirubin
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Bilirubin, direct measurement, Result
Item
Direct Bilirubin - Result
text
C0008000 (UMLS CUI [1,1])
C0201916 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Bilirubin, direct measurement, Result, Unit of Measure
Item
Direct Bilirubin - Units
text
C0008000 (UMLS CUI [1,1])
C0201916 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Bilirubin, direct measurement, Result, Lower limit of reference range
Item
Direct Bilirubin - Low
text
C0008000 (UMLS CUI [1,1])
C0201916 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Bilirubin, direct measurement, Result, Upper Limit of Normal
Item
Direct Bilirubin - High
text
C0008000 (UMLS CUI [1,1])
C0201916 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Bilirubin, direct measurement, Result, Toxicity Grade
Item
Direct Bilirubin - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0201916 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Total Bilirubin
text
C0008000 (UMLS CUI [1,1])
C0201913 (UMLS CUI [1,2])
Chemistry, Clinical, Bilirubin, total measurement
Code List
Total Bilirubin
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Bilirubin, total measurement, Result
Item
Total Bilirubin - Result
text
C0008000 (UMLS CUI [1,1])
C0201913 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Bilirubin, total measurement, Result, Unit of Measure
Item
Total Bilirubin - Units
text
C0008000 (UMLS CUI [1,1])
C0201913 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Bilirubin, total measurement, Result, Lower limit of reference range
Item
Total Bilirubin - Low
text
C0008000 (UMLS CUI [1,1])
C0201913 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Bilirubin, total measurement, Result, Upper Limit of Normal
Item
Total Bilirubin - High
text
C0008000 (UMLS CUI [1,1])
C0201913 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Bilirubin, total measurement, Result, Toxicity Grade
Item
Total Bilirubin - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0201913 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Carbon Dioxide
text
C0008000 (UMLS CUI [1,1])
C0007012 (UMLS CUI [1,2])
Chemistry, Clinical, Carbon Dioxide
Code List
Carbon Dioxide
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Carbon Dioxide, Result
Item
Carbon Dioxide - Result
text
C0008000 (UMLS CUI [1,1])
C0007012 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Carbon Dioxide, Result, Unit of Measure
Item
Carbon Dioxide - Units
text
C0008000 (UMLS CUI [1,1])
C0007012 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Carbon Dioxide, Result, Lower limit of reference range
Item
Carbon Dioxide - Low
text
C0008000 (UMLS CUI [1,1])
C0007012 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Carbon Dioxide, Result, Upper Limit of Normal
Item
Carbon Dioxide - High
text
C0008000 (UMLS CUI [1,1])
C0007012 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Carbon Dioxide, Result, Toxicity Grade
Item
Carbon Dioxide - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0007012 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
BUN
text
C0008000 (UMLS CUI [1,1])
C0005845 (UMLS CUI [1,2])
Chemistry, Clinical, Blood urea nitrogen measurement
Code List
BUN
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Blood urea nitrogen measurement, Result
Item
BUN - Result
text
C0008000 (UMLS CUI [1,1])
C0005845 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Blood urea nitrogen measurement, Result, Unit of Measure
Item
BUN - Units
text
C0008000 (UMLS CUI [1,1])
C0005845 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Blood urea nitrogen measurement, Result, Lower limit of reference range
Item
BUN - Low
text
C0008000 (UMLS CUI [1,1])
C0005845 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Blood urea nitrogen measurement, Result, Upper Limit of Normal
Item
BUN - High
text
C0008000 (UMLS CUI [1,1])
C0005845 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Blood urea nitrogen measurement, Result, Toxicity Grade
Item
BUN - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0005845 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Calcium
text
C0008000 (UMLS CUI [1,1])
C0201925 (UMLS CUI [1,2])
Chemistry, Clinical, Calcium measurement
Code List
Calcium
CL Item
No result (1)
CL Item
Results (2)
Chemistry, Clinical, Calcium measurement, Result
Item
Calcium - Result
text
C0008000 (UMLS CUI [1,1])
C0201925 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Calcium measurement, Result, Unit of Measure
Item
Calcium - Units
text
C0008000 (UMLS CUI [1,1])
C0201925 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Calcium measurement, Result, Lower limit of reference range
Item
Calcium - Low
text
C0008000 (UMLS CUI [1,1])
C0201925 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Calcium measurement, Result, Upper Limit of Normal
Item
Calcium - High
text
C0008000 (UMLS CUI [1,1])
C0201925 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Calcium measurement, Result, Toxicity Grade
Item
Calcium - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0201925 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Creatinine
text
C0008000 (UMLS CUI [1,1])
C0201975 (UMLS CUI [1,2])
Chemistry, Clinical, Creatinine measurement
Code List
Creatinine
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Creatinine measurement, Result
Item
Creatinine - Result
text
C0008000 (UMLS CUI [1,1])
C0201975 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Creatinine measurement, Result, Unit of Measure
Item
Creatinine - Units
text
C0008000 (UMLS CUI [1,1])
C0201975 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Creatinine measurement, Result, Lower limit of reference range
Item
Creatinine - Low
text
C0008000 (UMLS CUI [1,1])
C0201975 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Creatinine measurement, Result, Upper Limit of Normal
Item
Creatinine - High
text
C0008000 (UMLS CUI [1,1])
C0201975 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Creatinine measurement, Result, Toxicity Grade
Item
Creatinine - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0201975 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Magnesium
text
C0008000 (UMLS CUI [1,1])
C0373675 (UMLS CUI [1,2])
Chemistry, Clinical, Magnesium measurement
Code List
Magnesium
CL Item
No results (1)
CL Item
Results (2)
Item
Magnesium - Result
text
C0008000 (UMLS CUI [1,1])
C0373675 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Magnesium measurement
Code List
Magnesium - Result
Chemistry, Clinical, Magnesium measurement, Result, Unit of Measure
Item
Magnesium - Units
text
C0008000 (UMLS CUI [1,1])
C0373675 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Item
Magnesium - Low
text
C0008000 (UMLS CUI [1,1])
C0373675 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Magnesium measurement
Code List
Magnesium - Low
Item
Magnesium - High
text
C0008000 (UMLS CUI [1,1])
C0373675 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Magnesium measurement
Code List
Magnesium - High
Chemistry, Clinical, Magnesium measurement, Result, Toxicity Grade
Item
Magnesium - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0373675 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Potassium
text
C0008000 (UMLS CUI [1,1])
C0202194 (UMLS CUI [1,2])
Chemistry, Clinical, Potassium measurement
Code List
Potassium
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Potassium measurement, Result
Item
Potassium - Result
text
C0008000 (UMLS CUI [1,1])
C0202194 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Potassium measurement, Result, Unit of Measure
Item
Potassium - Units
text
C0008000 (UMLS CUI [1,1])
C0202194 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Potassium measurement, Result, Lower limit of reference range
Item
Potassium - Low
text
C0008000 (UMLS CUI [1,1])
C0202194 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Potassium measurement, Result, Upper Limit of Normal
Item
Potassium - High
text
C0008000 (UMLS CUI [1,1])
C0202194 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Potassium measurement, Result, Toxicity Grade
Item
Potassium - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0202194 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Sodium
text
C0008000 (UMLS CUI [1,1])
C0337443 (UMLS CUI [1,2])
Chemistry, Clinical, Sodium measurement
Code List
Sodium
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Sodium measurement, Result
Item
Sodium - Result
text
C0008000 (UMLS CUI [1,1])
C0337443 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Sodium measurement, Result, Unit of Measure
Item
Sodium - Units
text
C0008000 (UMLS CUI [1,1])
C0337443 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Sodium measurement, Result, Lower limit of reference range
Item
Sodium - Low
text
C0008000 (UMLS CUI [1,1])
C0337443 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Sodium measurement, Result, Upper Limit of Normal
Item
Sodium - High
text
C0008000 (UMLS CUI [1,1])
C0337443 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Sodium measurement, Result, Toxicity Grade
Item
Sodium - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0337443 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
H. pylori serology (IgG)
text
C0008000 (UMLS CUI [1,1])
C0079488 (UMLS CUI [1,2])
Chemistry, Clinical, Helicobacter pylori
Code List
H. pylori serology (IgG)
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Helicobacter pylori, Result
Item
H. pylori serology (IgG) - Result
text
C0008000 (UMLS CUI [1,1])
C0079488 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Helicobacter pylori, Result, Unit of Measure
Item
H. pylori serology (IgG) - Units
text
C0008000 (UMLS CUI [1,1])
C0079488 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Helicobacter pylori, Result, Lower limit of reference range
Item
H. pylori serology (IgG) - Low
text
C0008000 (UMLS CUI [1,1])
C0079488 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Helicobacter pylori, Result, Upper Limit of Normal
Item
H. pylori serology (IgG) - High
text
C0008000 (UMLS CUI [1,1])
C0079488 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Helicobacter pylori, Result, Toxicity Grade
Item
H. pylori serology (IgG) - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0079488 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Creatinine Clearance
text
C0008000 (UMLS CUI [1,1])
C0373595 (UMLS CUI [1,2])
Chemistry, Clinical, Creatinine clearance measurement
Code List
Creatinine Clearance
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Creatinine clearance measurement, Result
Item
Creatinine Clearance - Result
text
C0008000 (UMLS CUI [1,1])
C0373595 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Creatinine clearance measurement, Result, Unit of Measure
Item
Creatinine Clearance - Units
text
C0008000 (UMLS CUI [1,1])
C0373595 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Creatinine clearance measurement, Result, Lower limit of reference range
Item
Creatinine Clearance - Low
text
C0008000 (UMLS CUI [1,1])
C0373595 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Creatinine clearance measurement, Result, Upper Limit of Normal
Item
Creatinine Clearance - High
text
C0008000 (UMLS CUI [1,1])
C0373595 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Creatinine clearance measurement, Result, Toxicity Grade
Item
Creatinine Clearance - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0373595 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Laboratory Procedures, Chemistry, Clinical, Laboratory, Other
Item
Was any test on this page performed at a different lab than specified on this page?
text
C0022885 (UMLS CUI [1,1])
C0008000 (UMLS CUI [1,2])
C0022877 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
Item Group
Local Laboratory - Haematology
C0022885 (UMLS CUI-1)
C0474523 (UMLS CUI-2)
Laboratory, Hematology finding
Item
Laboratory Used For This Sample
text
C0022877 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
Laboratory Procedures, Hematology finding, Gender
Item
Gender used to determine lab normals
text
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C0079399 (UMLS CUI [1,3])
Laboratory Procedures, Hematology finding, Patient date of birth
Item
Date of birth used to determine lab normals
date
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C0421451 (UMLS CUI [1,3])
Laboratory Procedures, Hematology finding, Sampling, Date in time
Item
Date sample taken
date
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C0870078 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
Item
RBC
text
C0474523 (UMLS CUI [1,1])
C0014772 (UMLS CUI [1,2])
Hematology finding, Red Blood Cell Count measurement
Code List
RBC
CL Item
No result (1)
CL Item
Results (2)
Hematology finding, Red Blood Cell Count measurement, Result
Item
RBC - Result
text
C0474523 (UMLS CUI [1,1])
C0014772 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Hematology finding, Red Blood Cell Count measurement, Result, Unit of Measure
Item
RBC - Units
text
C0474523 (UMLS CUI [1,1])
C0014772 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Hematology finding, Red Blood Cell Count measurement, Result, Lower limit of reference range
Item
RBC - Low
text
C0474523 (UMLS CUI [1,1])
C0014772 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Hematology finding, Red Blood Cell Count measurement, Result, Upper Limit of Normal
Item
RBC - High
text
C0474523 (UMLS CUI [1,1])
C0014772 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Hematology finding, Red Blood Cell Count measurement, Result, Toxicity Grade
Item
RBC - Tox Grade
text
C0474523 (UMLS CUI [1,1])
C0014772 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Haemoglobin
text
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
Hematology finding, Hemoglobin
Code List
Haemoglobin
CL Item
No result (1)
CL Item
Results (2)
Hematology finding, Hemoglobin, Result
Item
Haemoglobin - Result
text
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Hematology finding, Hemoglobin, Result, Unit of Measure
Item
Haemoglobin - Units
text
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Hematology finding, Hemoglobin, Result, Lower limit of reference range
Item
Haemoglobin - Low
text
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Hematology finding, Hemoglobin, Result, Upper Limit of Normal
Item
Haemoglobin - High
text
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Hematology finding, Hemoglobin, Result, Toxicity Grade
Item
Haemoglobin - Tox Grade
text
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Haematocrit
text
C0474523 (UMLS CUI [1,1])
C0518014 (UMLS CUI [1,2])
Hematology finding, Hematocrit level
Code List
Haematocrit
CL Item
No result (1)
CL Item
Results (2)
Hematology finding, Hematocrit level, Result
Item
Haematocrit - Result
text
C0474523 (UMLS CUI [1,1])
C0518014 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Hematology finding, Hematocrit level, Result, Unit of Measure
Item
Haematocrit - Units
text
C0474523 (UMLS CUI [1,1])
C0518014 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Hematology finding, Hematocrit level, Result, Lower limit of reference range
Item
Haematocrit - Low
text
C0474523 (UMLS CUI [1,1])
C0518014 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Hematology finding, Hematocrit level, Result, Upper Limit of Normal
Item
Haematocrit - High
text
C0474523 (UMLS CUI [1,1])
C0518014 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Hematology finding, Hematocrit level, Result, Toxicity Grade
Item
Haematocrit - Tox Grade
text
C0474523 (UMLS CUI [1,1])
C0518014 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Platelets
text
C0474523 (UMLS CUI [1,1])
C0005821 (UMLS CUI [1,2])
Hematology finding, Blood Platelets
Code List
Platelets
CL Item
No result (1)
CL Item
Results (2)
Hematology finding, Blood Platelets, Result
Item
Platelets - Result
text
C0474523 (UMLS CUI [1,1])
C0005821 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Hematology finding, Blood Platelets, Result, Unit of Measure
Item
Platelets - Units
text
C0474523 (UMLS CUI [1,1])
C0005821 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Hematology finding, Blood Platelets, Result, Lower limit of reference range
Item
Platelets - Low
text
C0474523 (UMLS CUI [1,1])
C0005821 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Hematology finding, Blood Platelets, Result, Upper Limit of Normal
Item
Platelets - High
text
C0474523 (UMLS CUI [1,1])
C0005821 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Hematology finding, Blood Platelets, Result, Toxicity Grade
Item
Platelets - Tox Grade
text
C0474523 (UMLS CUI [1,1])
C0005821 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
WBC
text
C0474523 (UMLS CUI [1,1])
C0023508 (UMLS CUI [1,2])
Hematology finding, White Blood Cell Count procedure
Code List
WBC
CL Item
No result (1)
CL Item
Results (2)
Hematology finding, White Blood Cell Count procedure, Result
Item
WBC - Result
text
C0474523 (UMLS CUI [1,1])
C0023508 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Hematology finding, White Blood Cell Count procedure, Result, Unit of Measure
Item
WBC - Units
text
C0474523 (UMLS CUI [1,1])
C0023508 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Hematology finding, White Blood Cell Count procedure, Result, Lower limit of reference range
Item
WBC - Low
text
C0474523 (UMLS CUI [1,1])
C0023508 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Hematology finding, White Blood Cell Count procedure, Result, Upper Limit of Normal
Item
WBC - High
text
C0474523 (UMLS CUI [1,1])
C0023508 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Hematology finding, White Blood Cell Count procedure, Result, Toxicity Grade
Item
WBC - Tox Grade
text
C0474523 (UMLS CUI [1,1])
C0023508 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Differential Units
text
C0474523 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Hematology finding, Unit of Measure
Code List
Differential Units
CL Item
Precent (1)
CL Item
Absolute count (2)
Item
Basophils
text
C0474523 (UMLS CUI [1,1])
C0200641 (UMLS CUI [1,2])
Hematology finding, Blood basophil count (lab test)
Code List
Basophils
CL Item
No result (1)
CL Item
Results (2)
Hematology finding, Blood basophil count (lab test), Result
Item
Basophils - Result
text
C0474523 (UMLS CUI [1,1])
C0200641 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Hematology finding, Blood basophil count (lab test), Result, Unit of Measure
Item
Basophils - Units
text
C0474523 (UMLS CUI [1,1])
C0200641 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Hematology finding, Blood basophil count (lab test), Result, Lower limit of reference range
Item
Basophils - Low
text
C0474523 (UMLS CUI [1,1])
C0200641 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Hematology finding, Blood basophil count (lab test), Result, Upper Limit of Normal
Item
Basophils - High
text
C0474523 (UMLS CUI [1,1])
C0200641 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Hematology finding, Blood basophil count (lab test), Result, Toxicity Grade
Item
Basophils - Tox Grade
text
C0474523 (UMLS CUI [1,1])
C0200641 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Eosinophils
text
C0474523 (UMLS CUI [1,1])
C0200638 (UMLS CUI [1,2])
Hematology finding, Eosinophil count procedure
Code List
Eosinophils
CL Item
No result (1)
CL Item
Results (2)
Hematology finding, Eosinophil count procedure, Result
Item
Eosinophils - Result
text
C0474523 (UMLS CUI [1,1])
C0200638 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Hematology finding, Eosinophil count procedure, Result, Unit of Measure
Item
Eosinophils - Units
text
C0474523 (UMLS CUI [1,1])
C0200638 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Hematology finding, Eosinophil count procedure, Result, Lower limit of reference range
Item
Eosinophils - Low
text
C0474523 (UMLS CUI [1,1])
C0200638 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Hematology finding, Eosinophil count procedure, Result, Upper Limit of Normal
Item
Eosinophils - High
text
C0474523 (UMLS CUI [1,1])
C0200638 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Hematology finding, Eosinophil count procedure, Result, Toxicity Grade
Item
Eosinophils - Tox Grade
text
C0474523 (UMLS CUI [1,1])
C0200638 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Lymphocytes
text
C0474523 (UMLS CUI [1,1])
C0200635 (UMLS CUI [1,2])
Hematology finding, Lymphocyte Count measurement
Code List
Lymphocytes
CL Item
No result (1)
CL Item
Results (2)
Hematology finding, Lymphocyte Count measurement, Result
Item
Lymphocytes - Result
text
C0474523 (UMLS CUI [1,1])
C0200635 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Hematology finding, Lymphocyte Count measurement, Result, Unit of Measure
Item
Lymphocytes - Units
text
C0474523 (UMLS CUI [1,1])
C0200635 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Hematology finding, Lymphocyte Count measurement, Result, Lower limit of reference range
Item
Lymphocytes - Low
text
C0474523 (UMLS CUI [1,1])
C0200635 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Hematology finding, Lymphocyte Count measurement, Result, Upper Limit of Normal
Item
Lymphocytes - High
text
C0474523 (UMLS CUI [1,1])
C0200635 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Hematology finding, Lymphocyte Count measurement, Result, Toxicity Grade
Item
Lymphocytes - Tox Grade
text
C0474523 (UMLS CUI [1,1])
C0200635 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Monocytes
text
C0474523 (UMLS CUI [1,1])
C0750880 (UMLS CUI [1,2])
Hematology finding, Monocyte count result
Code List
Monocytes
CL Item
No result (1)
CL Item
Results (2)
Hematology finding, Monocyte count result, Result
Item
Monocytes - Result
text
C0474523 (UMLS CUI [1,1])
C0750880 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Hematology finding, Monocyte count result, Result, Unit of Measure
Item
Monocytes - Units
text
C0474523 (UMLS CUI [1,1])
C0750880 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Hematology finding, Monocyte count result, Result, Lower limit of reference range
Item
Monocytes - Low
text
C0474523 (UMLS CUI [1,1])
C0750880 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Hematology finding, Monocyte count result, Result, Upper Limit of Normal
Item
Monocytes - High
text
C0474523 (UMLS CUI [1,1])
C0750880 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Hematology finding, Monocyte count result, Result, Toxicity Grade
Item
Monocytes - Tox Grade
text
C0474523 (UMLS CUI [1,1])
C0750880 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Neutrophils
text
C0474523 (UMLS CUI [1,1])
C0948762 (UMLS CUI [1,2])
Hematology finding, Absolute neutrophil count
Code List
Neutrophils
CL Item
No result (1)
CL Item
Results (2)
Hematology finding, Absolute neutrophil count, Result
Item
Neutrophils - Result
text
C0474523 (UMLS CUI [1,1])
C0948762 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Hematology finding, Absolute neutrophil count, Result, Unit of Measure
Item
Neutrophils - Units
text
C0474523 (UMLS CUI [1,1])
C0948762 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Hematology finding, Absolute neutrophil count, Result, Lower limit of reference range
Item
Neutrophils - Low
text
C0474523 (UMLS CUI [1,1])
C0948762 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Hematology finding, Absolute neutrophil count, Result, Upper Limit of Normal
Item
Neutrophils - High
text
C0474523 (UMLS CUI [1,1])
C0948762 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Hematology finding, Absolute neutrophil count, Result, Toxicity Grade
Item
Neutrophils - Tox Grade
text
C0474523 (UMLS CUI [1,1])
C0948762 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Laboratory Procedures, Hematology finding, Laboratory, Other
Item
Was any test on this page performed at a different lab than specified on this page?
text
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C0022877 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
Item Group
Subject Identification
C2348585 (UMLS CUI-1)
Clinical Trial Subject Unique Identifier
Item
Subject number
integer
C2348585 (UMLS CUI [1])
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