ID

40893

Descripción

Study ID: 111155 Clinical Study ID: 111155 Study Title: A double blind, parallel group, placebo controlled study to evaluate the effect of a single oral dose of GSK958108 on ejaculatory latency time (ELT) in male patients suffering from premature ejaculation. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00861484 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: GSK958108 , Placebo Trade Name: N/A Study Indication: Premature Ejaculation

Palabras clave

Versiones (1)
  1. 31/5/20 31/5/20 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

31 de mayo de 2020

DOI

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Licencia

Creative Commons BY-NC 4.0
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Effect of GSK958108 on ejaculatory latency time (ELT); NCT00861484

Inglés

Screen

1 formularios  
  1. StudyEvent: ODM
    1. Screen
Inform Screening
Descripción

Inform Screening

Alias
UMLS CUI-1
C0220908
Subject initials
Descripción

Clinical trial participant (person), Person Initials

Tipo de datos

text

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

Patient date of birth

Tipo de datos

date

Alias
UMLS CUI [1]
C0421451
Inform Enrollment
Descripción

Inform Enrollment

Alias
UMLS CUI-1
C1516879
Subject number
Descripción

Clinical Trial Subject Unique Identifier

Tipo de datos

text

Alias
UMLS CUI [1]
C2348585
Date of Visit
Descripción

Date of Visit

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

Date of visit, Assessment Date

Tipo de datos

date

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

Demography

Alias
UMLS CUI-1
C0011298
Date of birth
Descripción

Patient date of birth

Tipo de datos

date

Alias
UMLS CUI [1]
C0421451
Sex
Descripción

Gender

Tipo de datos

text

Alias
UMLS CUI [1]
C0079399
Ethnicity
Descripción

Ethnic group

Tipo de datos

text

Alias
UMLS CUI [1]
C0015031
Geographic ancestry
Descripción

Your ancestry or national origin

Tipo de datos

text

Alias
UMLS CUI [1]
C3841890
Eligibility Question
Descripción

Eligibility Question

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

Eligibility Determination

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013893
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI-1
C1512693
Male between 18 and 50 years of age.
Descripción

Gender, Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
Body weight ≥ 50 kg (110 lbs) and BMI within the range 19.0 – 29.9 kg/m2 inclusive).
Descripción

Body Weight; Body mass index

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0005910
UMLS CUI [2]
C1305855
Heterosexual orientation
Descripción

Heterosexuality

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0019421
Long term symptoms of PE that meet DSM-IV-TR criteria for PE: a. Persistent or recurrent ejaculation with minimal sexual stimulation before, on or shortly after penetration and before the person wishes it. The clinician must take into account factors that affect duration of the excitement phase, such as age, novelty of the sexual partner or situation, and recent frequency of sexual activity. b. The disturbance causes marked distress or interpersonal difficulty. c. The premature ejaculation is not due exclusively to the direct effects of a substance (e.g., withdrawal from opioids).
Descripción

Premature Ejaculation, Symptoms

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0033038
UMLS CUI [1,2]
C1457887
Premature ejaculation is not due to any other concomitant medical condition
Descripción

Premature Ejaculation, Primary disorders

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0033038
UMLS CUI [1,2]
C0277554
Self-reported moderate or severe primary PE prior to screening with ejaculation occurring on or before penetration, or shortly there after with minimal stimulation.
Descripción

Premature Ejaculation

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0033038
The patient has a baseline ELT less than 3 minutes.
Descripción

Premature Ejaculation, Response Latency, Time

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0033038
UMLS CUI [1,2]
C0242465
UMLS CUI [1,3]
C0040223
Subjects must agree to use one of the contraception methods listed in Section 8.1. This criterion must be followed from the time of the first dose of study medication until 3 months after last dose.
Descripción

Contraceptive methods

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0700589
Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
The subject is able to cooperate in all part of the eye examination (including dilation with mydriatics).
Descripción

Ophthalmic examination and evaluation, Cooperation

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0392337
The subject has a visual acuity that is equivalent to 20/30 in each eye, with appropriate correction if needed.
Descripción

Visual Acuity

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0042812
QTcB o rQTcF < 450 msec.
Descripción

QTcB - Bazett's Correction Formula; QTcF - Fridericia's Correction Formula

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1882512
UMLS CUI [2]
C1882513
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI-1
C0680251
Erectile dysfunction. Erectile Function domain of International Index of Erectile Function questionnaire < 26.
Descripción

Erectile dysfunction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0242350
Any clinically relevant abnormality identified on the screening examination or any other medical condition or circumstance making the volunteer unsuitable for participation in the study.
Descripción

Other medical condition

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3843040
The subject has a history of migraine.
Descripción

Migraine Disorders, Medical History

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0149931
UMLS CUI [1,2]
C0262926
The subject has a history of psychiatric illness, except for those symptoms related to their PE.
Descripción

Mental disorders, Medical History

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0004936
UMLS CUI [1,2]
C0262926
Any history of suicidal attempts or behaviour.
Descripción

Suicidal behavior, Medical History; Suicide attempt, Medical History

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1760428
UMLS CUI [1,2]
C0262926
UMLS CUI [2,1]
C0038663
UMLS CUI [2,2]
C0262926
The subject has a history of any eye disorder or is colour blind, excluding myopia and presbyopia.
Descripción

Disorder of eye, Medical History; Color blindness

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0015397
UMLS CUI [1,2]
C0262926
UMLS CUI [2]
C0242225
History of long QT syndrome (personal or family) or other cardiac conduction disorder, or other clinically significant cardiac disease.
Descripción

Long QT Syndrome; Cardiac conduction abnormality; Heart Diseases

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023976
UMLS CUI [2]
C1842820
UMLS CUI [3]
C0018799
A positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening (with the exception of phase I hepatic impairment studies, oncology studies, hepatitis, hepatic fibrosis, or HIV studies).
Descripción

Hepatitis B surface antigen positive; Hepatitis C antibody positive

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0149709
UMLS CUI [2]
C0281863
A positive test for HIV antibody.
Descripción

HIV antibody positive

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0920548
History of sensitivity or intolerance to drugs that effect serotonin, including serotonin-reuptake inhibitors (SSRIs), or a history of drug or other allergy that, in the opinion of the investigator or GSK Medical Monitor, contraindicates their participation.
Descripción

Medical History, Hypersensitivity, Drug intolerance

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0020517
UMLS CUI [1,3]
C0277585
History of regular alcohol consumption within 6 months of the study defined as: an average weekly intake of greater than 21 units or an average daily intake of greater than 3 units. One unit is equivalent to a half-pint (220mL) of beer or 1 (25ml) measure of spirits or 1 glass (125ml) of wine.
Descripción

Alcohol consumption

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001948
The subject has a positive pre-study drug/alcohol screen. A minimum list of drugs that will be screened for include amphetamines, barbiturates, cocaine, opiates, cannabinoids and benzodiazepines (can be repeated once at screening).
Descripción

Drug screen positive; Alcohol consumption screening, Positive Finding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0743295
UMLS CUI [2,1]
C0420032
UMLS CUI [2,2]
C1514241
Subject smokes more than 10 cigarettes per day.
Descripción

Tobacco use

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0543414
Consumption of red wine, seville oranges, grapefruit or grapefruit juice [and/or pummelos, exotic citrus fruits, grapefruit hybrids] from 7 days prior to the first dose of study medication.
Descripción

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

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0349371
UMLS CUI [2]
C0330922
UMLS CUI [3]
C0995150
UMLS CUI [4]
C0452456
Regular use of any PDE-5 inhibitors.
Descripción

Phosphodiesterase 5 inhibitor

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1318700
Subject has received or is continuing to receive any treatment for PE (e.g.local anaesthetic spray, or intra-cavernosal injection) in the four weeks prior to the study start.
Descripción

Premature Ejaculation, Therapeutic procedure

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0033038
UMLS CUI [1,2]
C0087111
Use of prescription or non-prescription drugs, including vitamins, herbal and dietary supplements (including St John’s Wort) within 7 days (or 14 days if the drug is a potential enzyme inducer) or 5 half-lives (whichever is longer) prior to the first dose of study medication, unless in the opinion of the Investigator and GSK Medical Monitor the medication will not interfere with the study procedures or compromise subject safety.
Descripción

Medication use, Vitamins, Herbal

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013227
UMLS CUI [2]
C0042890
UMLS CUI [3]
C1504473
UMLS CUI [4]
C0242295
The subject has participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer).
Descripción

Study Subject Participation Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
Exposure to more than four new chemical entities within 12 months prior to the first dosing day.
Descripción

Investigational New Drugs

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013230
Where participation in the study would result in donation of blood or blood products in excess of 500 mL within a 56 day period.
Descripción

Blood Donation

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0005794
Unwillingness or inability to follow the procedures outlined in the protocol.
Descripción

Protocol Compliance

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0525058
Subject Identification
Descripción

Subject Identification

Alias
UMLS CUI-1
C2348585
Subject number
Descripción

Clinical Trial Subject Unique Identifier

Tipo de datos

integer

Alias
UMLS CUI [1]
C2348585
Vital Signs
Descripción

Vital Signs

Alias
UMLS CUI-1
C0518766
Semi-supine - Actual date/time
Descripción

Vital signs, Semi-erect, Date in time, Time

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C0518766
UMLS CUI [1,2]
C0522019
UMLS CUI [1,3]
C0011008
UMLS CUI [1,4]
C0040223
Height
Descripción

Body Height

Tipo de datos

integer

Unidades de medida
  • cm
Alias
UMLS CUI [1]
C0005890
cm
Weight
Descripción

Body Weight

Tipo de datos

float

Unidades de medida
  • kg
Alias
UMLS CUI [1]
C0005910
kg
Body mass index
Descripción

Body mass index

Tipo de datos

float

Alias
UMLS CUI [1]
C1305855
Semi-supine - Blood pressure - Systolic
Descripción

Systolic Pressure, Semi-erect

Tipo de datos

integer

Unidades de medida
  • mmHg
Alias
UMLS CUI [1,1]
C0871470
UMLS CUI [1,2]
C0522019
mmHg
Semi-supine - Blood pressure - Diastolic
Descripción

Diastolic blood pressure, Semi-erect

Tipo de datos

integer

Unidades de medida
  • mmHg
Alias
UMLS CUI [1,1]
C0428883
UMLS CUI [1,2]
C0522019
mmHg
Semi-supine - Heart rate
Descripción

Heart rate, Semi-erect

Tipo de datos

integer

Unidades de medida
  • bpm
Alias
UMLS CUI [1,1]
C0018810
UMLS CUI [1,2]
C0522019
bpm
Semi-supine - Respiration rate
Descripción

Respiratory rate, Semi-erect

Tipo de datos

integer

Unidades de medida
  • breaths/min
Alias
UMLS CUI [1,1]
C0231832
UMLS CUI [1,2]
C0522019
breaths/min
Standing - Actual date/time
Descripción

Vital signs, Erect, Date in time, Time

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C0518766
UMLS CUI [1,2]
C0522014
UMLS CUI [1,3]
C0011008
UMLS CUI [1,4]
C0040223
Standing - Blood pressure - Systolic
Descripción

Systolic Pressure, Erect

Tipo de datos

integer

Unidades de medida
  • mmHg
Alias
UMLS CUI [1,1]
C0871470
UMLS CUI [1,2]
C0522014
mmHg
Standing - Blood pressure - Diastolic
Descripción

Diastolic blood pressure, Erect

Tipo de datos

integer

Unidades de medida
  • mmHg
Alias
UMLS CUI [1,1]
C0428883
UMLS CUI [1,2]
C0522014
mmHg
Standing - Heart rate
Descripción

Heart rate, Erect

Tipo de datos

integer

Unidades de medida
  • bpm
Alias
UMLS CUI [1,1]
C0018810
UMLS CUI [1,2]
C0522014
bpm
12-Lead ECG
Descripción

12-Lead ECG

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

12 lead ECG, Date in time, Time

Tipo de datos

datetime

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

12 lead ECG, Heart rate

Tipo de datos

integer

Unidades de medida
  • bpm
Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C0018810
bpm
PR Interval
Descripción

12 lead ECG, Electrocardiogram: P-R interval

Tipo de datos

integer

Unidades de medida
  • msec
Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C0429087
msec
QRS Duration
Descripción

12 lead ECG, QRS complex duration

Tipo de datos

integer

Unidades de medida
  • msec
Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C0429025
msec
Uncorrected QT Interval
Descripción

12 lead ECG, QT interval - finding

Tipo de datos

integer

Unidades de medida
  • msec
Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C1287082
msec
QTc Interval
Descripción

12 lead ECG, Electrocardiogram QT corrected interval

Tipo de datos

integer

Unidades de medida
  • msec
Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C0855331
Method of QTc Calculation
Descripción

12 lead ECG, Electrocardiogram QT corrected interval, Evaluation Method

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C0855331
UMLS CUI [1,3]
C2911685
Result of the ECG
Descripción

12 lead ECG, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C1274040
Local Laboratory - Haematology
Descripción

Local Laboratory - Haematology

Alias
UMLS CUI-1
C0022885
UMLS CUI-2
C0474523
Date and time sample taken
Descripción

Hematology, Sampling, Date in time, Time

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0870078
UMLS CUI [1,3]
C0011008
UMLS CUI [1,4]
C0040223
Haemoglobin
Descripción

Hematology finding, Hemoglobin

Tipo de datos

text

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

Hematology finding, Hemoglobin, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0474523
UMLS CUI [1,3]
C1274040
RBC
Descripción

Hematology finding, Red Blood Cell Count measurement

Tipo de datos

text

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

Hematology finding, Red Blood Cell Count measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0014772
UMLS CUI [1,3]
C1274040
MCV
Descripción

Hematology finding, Erythrocyte Mean Corpuscular Volume Measurement

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C1948043
MCV - Result
Descripción

Hematology finding, Erythrocyte Mean Corpuscular Volume Measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C1948043
UMLS CUI [1,3]
C1274040
MCH
Descripción

Hematology finding, Erythrocyte Mean Corpuscular Hemoglobin Test

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0369183
MCH - Result
Descripción

Hematology finding, Erythrocyte Mean Corpuscular Hemoglobin Test, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0369183
UMLS CUI [1,3]
C1274040
MCHC
Descripción

Hematology finding, Mean corpuscular hemoglobin concentration determination

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0474535
MCHC - Result
Descripción

Hematology finding, Mean corpuscular hemoglobin concentration determination, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0474535
UMLS CUI [1,3]
C1274040
Platelets
Descripción

Hematology finding, Blood Platelets

Tipo de datos

text

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

Hematology finding, Blood Platelets, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0005821
UMLS CUI [1,3]
C1274040
WBC
Descripción

Hematology finding, White Blood Cell Count procedure

Tipo de datos

text

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

Hematology finding, White Blood Cell Count procedure, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0023508
UMLS CUI [1,3]
C1274040
Neutrophils
Descripción

Hematology finding, Absolute neutrophil count

Tipo de datos

text

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

Hematology finding, Absolute neutrophil count, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0948762
UMLS CUI [1,3]
C1274040
Lymphocytes
Descripción

Hematology finding, Lymphocyte Count measurement

Tipo de datos

text

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

Hematology finding, Lymphocyte Count measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200635
UMLS CUI [1,3]
C1274040
Monocytes
Descripción

Hematology finding, Monocyte count result

Tipo de datos

text

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

Hematology finding, Monocyte count result, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0750880
UMLS CUI [1,3]
C1274040
Eosinophils
Descripción

Hematology finding, Eosinophil count procedure

Tipo de datos

text

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

Hematology finding, Eosinophil count procedure, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200638
UMLS CUI [1,3]
C1274040
Basophils
Descripción

Hematology finding, Blood basophil count (lab test)

Tipo de datos

text

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

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

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0200641
UMLS CUI [1,3]
C1274040
Reticulocytes
Descripción

Hematology finding, Reticulocyte count (procedure)

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0206161
Reticulocytes - Result
Descripción

Hematology finding, Reticulocyte count (procedure), Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0206161
UMLS CUI [1,3]
C1274040
Local Laboratory - Clinical Chemistry
Descripción

Local Laboratory - Clinical Chemistry

Alias
UMLS CUI-1
C0022885
UMLS CUI-2
C0008000
Date and time sample taken
Descripción

Chemistry, Clinical, Sampling, Date in time, Time

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0870078
UMLS CUI [1,3]
C0011008
UMLS CUI [1,4]
C0040223
Urea
Descripción

Chemistry, Clinical, Urea measurement

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0523961
Urea - Result
Descripción

Chemistry, Clinical, Urea measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0523961
UMLS CUI [1,3]
C1274040
Creatinine
Descripción

Chemistry, Clinical, Creatinine measurement

Tipo de datos

text

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

Chemistry, Clinical, Creatinine measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201975
UMLS CUI [1,3]
C1274040
Total Bilirubin
Descripción

Chemistry, Clinical, Bilirubin, total measurement

Tipo de datos

text

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

Chemistry, Clinical, Bilirubin, total measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201913
UMLS CUI [1,3]
C1274040
Direct Bilirubin
Descripción

Chemistry, Clinical, Bilirubin, direct measurement

Tipo de datos

text

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

Chemistry, Clinical, Bilirubin, direct measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201916
UMLS CUI [1,3]
C1274040
Calcium
Descripción

Chemistry, Clinical, Calcium measurement

Tipo de datos

text

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

Chemistry, Clinical, Calcium measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201925
UMLS CUI [1,3]
C1274040
Chloride
Descripción

Chemistry, Clinical, Chloride measurement

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201952
Chloride - Result
Descripción

Chemistry, Clinical, Chloride measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201952
UMLS CUI [1,3]
C1274040
Potassium
Descripción

Chemistry, Clinical, Potassium measurement

Tipo de datos

text

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

Chemistry, Clinical, Potassium measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0202194
UMLS CUI [1,3]
C1274040
Sodium
Descripción

Chemistry, Clinical, Sodium measurement

Tipo de datos

text

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

Chemistry, Clinical, Sodium measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0337443
UMLS CUI [1,3]
C1274040
Uric Acid
Descripción

Chemistry, Clinical, Uric Acid

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0041980
Uric Acid - Result
Descripción

Chemistry, Clinical, Uric Acid, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0041980
UMLS CUI [1,3]
C1274040
Glucose
Descripción

Chemistry, Clinical, Glucose measurement

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0337438
Glucose - Result
Descripción

Chemistry, Clinical, Glucose measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0337438
UMLS CUI [1,3]
C1274040
Albumin
Descripción

Chemistry, Clinical, Albumin measurement

Tipo de datos

text

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

Chemistry, Clinical, Albumin measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201838
UMLS CUI [1,3]
C1274040
Total Protein
Descripción

Chemistry, Clinical, Total protein measurement

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0555903
Total Protein - Result
Descripción

Chemistry, Clinical, Total protein measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0555903
UMLS CUI [1,3]
C1274040
AST
Descripción

Chemistry, Clinical, Aspartate aminotransferase measurement

Tipo de datos

text

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

Chemistry, Clinical, Aspartate aminotransferase measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201899
UMLS CUI [1,3]
C1274040
ALT
Descripción

Chemistry, Clinical, Alanine aminotransferase measurement

Tipo de datos

text

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

Chemistry, Clinical, Alanine aminotransferase measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201836
UMLS CUI [1,3]
C1274040
Alkaline Phosphatase
Descripción

Chemistry, Clinical, Alkaline phosphatase measurement

Tipo de datos

text

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

Chemistry, Clinical, Alkaline phosphatase measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0201850
UMLS CUI [1,3]
C1274040
Local Laboratory - Urinalysis
Descripción

Local Laboratory - Urinalysis

Alias
UMLS CUI-1
C0022885
UMLS CUI-2
C0042014
Date and time sample taken
Descripción

Urinalysis, Sampling, Date in time, Time

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C0042014
UMLS CUI [1,2]
C0870078
UMLS CUI [1,3]
C0011008
UMLS CUI [1,4]
C0040223
Result of dipstick
Descripción

Urinalysis, Urine dipstick test, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0042014
UMLS CUI [1,2]
C0430370
UMLS CUI [1,3]
C1274040
Was a sedimentary microscopy performed?
Descripción

Urinalysis, Urine Sediment Analysis Measurement

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0430397
UMLS CUI [1,2]
C2700128
pH
Descripción

Urinalysis, Urine dipstick test, Urine pH measurement

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0042014
UMLS CUI [1,2]
C0430370
UMLS CUI [1,3]
C0042044
pH - Result
Descripción

Urinalysis, Urine dipstick test, Urine pH measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0042014
UMLS CUI [1,2]
C0430370
UMLS CUI [1,3]
C0042044
UMLS CUI [1,4]
C1274040
Glucose
Descripción

Urinalysis, Urine dipstick test, Glucose measurement

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0042014
UMLS CUI [1,2]
C0430370
UMLS CUI [1,3]
C0004076
Glucose - Result
Descripción

Urinalysis, Urine dipstick test, Glucose measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0042014
UMLS CUI [1,2]
C0430370
UMLS CUI [1,3]
C0004076
UMLS CUI [1,4]
C1274040
Protein
Descripción

Urinalysis, Urine dipstick test, Urine protein test

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0042014
UMLS CUI [1,2]
C0430370
UMLS CUI [1,3]
C0262923
Protein - Result
Descripción

Urinalysis, Urine dipstick test, Urine protein test, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0042014
UMLS CUI [1,2]
C0430370
UMLS CUI [1,3]
C0262923
UMLS CUI [1,4]
C1274040
Blood
Descripción

Urinalysis, Urine dipstick test, Urine dipstick for blood

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0042014
UMLS CUI [1,2]
C0430370
UMLS CUI [1,3]
C0430372
Blood - Result
Descripción

Urinalysis, Urine dipstick test, Urine dipstick for blood, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0042014
UMLS CUI [1,2]
C0430370
UMLS CUI [1,3]
C0430372
UMLS CUI [1,4]
C1274040
Ketones
Descripción

Urinalysis, Urine dipstick test, Ketones/Urine

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0042014
UMLS CUI [1,2]
C0430370
UMLS CUI [1,3]
C1991100
Ketones - Result
Descripción

Urinalysis, Urine dipstick test, Ketones/Urine, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0042014
UMLS CUI [1,2]
C0430370
UMLS CUI [1,3]
C1991100
UMLS CUI [1,4]
C1274040
Specific Gravity
Descripción

Urinalysis, Urine dipstick test, Specific gravity measurement

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0042014
UMLS CUI [1,2]
C0430370
UMLS CUI [1,3]
C0202517
Specific Gravity - Result
Descripción

Urinalysis, Urine dipstick test, Specific gravity measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0042014
UMLS CUI [1,2]
C0430370
UMLS CUI [1,3]
C0202517
UMLS CUI [1,4]
C1274040
Date and time sample taken (Sediment microscopy)
Descripción

Urinalysis, Urine Sediment Analysis Measurement, Sampling, Date in time, Time

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C0042014
UMLS CUI [1,2]
C2700128
UMLS CUI [1,3]
C0870078
UMLS CUI [1,4]
C0011008
UMLS CUI [1,5]
C0040223
White blood cells
Descripción

Urinalysis, Urine Sediment Analysis Measurement, White Blood Cell Count procedure

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0430397
UMLS CUI [1,2]
C2700128
UMLS CUI [1,3]
C0023508
White blood cells - Result
Descripción

Urinalysis, Urine Sediment Analysis Measurement, White Blood Cell Count procedure, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0430397
UMLS CUI [1,2]
C2700128
UMLS CUI [1,3]
C0023508
UMLS CUI [1,4]
C1274040
Red blood cells
Descripción

Urinalysis, Urine Sediment Analysis Measurement, Red Blood Cell Count measurement

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0430397
UMLS CUI [1,2]
C2700128
UMLS CUI [1,3]
C0014772
Red blood cells - Result
Descripción

Urinalysis, Urine Sediment Analysis Measurement, Red Blood Cell Count measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0430397
UMLS CUI [1,2]
C2700128
UMLS CUI [1,3]
C0014772
UMLS CUI [1,4]
C1274040
Hyaline casts
Descripción

Urinalysis, Urine Sediment Analysis Measurement, Urine Hyaline Cast Test

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0430397
UMLS CUI [1,2]
C2700128
UMLS CUI [1,3]
C1254537
Hyaline casts - Result
Descripción

Urinalysis, Urine Sediment Analysis Measurement, Urine Hyaline Cast Test, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0430397
UMLS CUI [1,2]
C2700128
UMLS CUI [1,3]
C1254537
UMLS CUI [1,4]
C1274040
Cellular casts
Descripción

Urinalysis, Urine Sediment Analysis Measurement, Cellular Cast Measurement

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0430397
UMLS CUI [1,2]
C2700128
UMLS CUI [1,3]
C2699157
Cellular casts - Result
Descripción

Urinalysis, Urine Sediment Analysis Measurement, Cellular Cast Measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0430397
UMLS CUI [1,2]
C2700128
UMLS CUI [1,3]
C2699157
UMLS CUI [1,4]
C1274040
Local Laboratory - Hormones
Descripción

Local Laboratory - Hormones

Alias
UMLS CUI-1
C0022885
UMLS CUI-2
C0019932
Date and time sample taken
Descripción

Laboratory Procedures, Hormones, Sampling, Date in time, Time

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0019932
UMLS CUI [1,3]
C0870078
UMLS CUI [1,4]
C0011008
UMLS CUI [1,5]
C0040223
Total Testosterone
Descripción

Laboratory Procedures, Hormones, Total Testosterone Measurement

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0019932
UMLS CUI [1,3]
C0202227
Total Testosterone - Result
Descripción

Laboratory Procedures, Hormones, Total Testosterone Measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0019932
UMLS CUI [1,3]
C0202227
UMLS CUI [1,4]
C1274040
LH
Descripción

Laboratory Procedures, Hormones, Luteinizing hormone measurement

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0019932
UMLS CUI [1,3]
C0202123
LH - Result
Descripción

Laboratory Procedures, Hormones, Luteinizing hormone measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0019932
UMLS CUI [1,3]
C0202123
UMLS CUI [1,4]
C1274040
FSH
Descripción

Laboratory Procedures, Hormones, Follicle stimulating hormone measurement

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0019932
UMLS CUI [1,3]
C0202022
FSH - Result
Descripción

Laboratory Procedures, Hormones, Follicle stimulating hormone measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0019932
UMLS CUI [1,3]
C0202022
UMLS CUI [1,4]
C1274040
Local Laboratory - FTEST
Descripción

Local Laboratory - FTEST

Alias
UMLS CUI-1
C0022885
UMLS CUI-2
C0202228
Date and time sample taken
Descripción

Free Testosterone Measurement, Sampling, Date in time, Time

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C0202228
UMLS CUI [1,2]
C0870078
UMLS CUI [1,3]
C0011008
UMLS CUI [1,4]
C0040223
Free Testosterone
Descripción

Free Testosterone Measurement

Tipo de datos

text

Alias
UMLS CUI [1]
C0202228
Free Testosterone - Result
Descripción

Free Testosterone Measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0202228
UMLS CUI [1,2]
C1274040
Local Laboratory - Prolactin
Descripción

Local Laboratory - Prolactin

Alias
UMLS CUI-1
C0022885
UMLS CUI-2
C0373706
Prolactin 1 - Date and time sample taken
Descripción

Prolactin measurement, Sampling, Date in time, Time

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C0373706
UMLS CUI [1,2]
C0870078
UMLS CUI [1,3]
C0011008
UMLS CUI [1,4]
C0040223
Prolactin 1 - Prolactin
Descripción

Prolactin measurement

Tipo de datos

text

Alias
UMLS CUI [1]
C0373706
Prolactin 1 - Prolactin - Result
Descripción

Prolactin measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0373706
UMLS CUI [1,2]
C1274040
Prolactin 2 - Date and time sample taken
Descripción

Prolactin measurement, Sampling, Date in time, Time

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C0373706
UMLS CUI [1,2]
C0870078
UMLS CUI [1,3]
C0011008
UMLS CUI [1,4]
C0040223
Prolactin 2 - Prolactin
Descripción

Prolactin measurement

Tipo de datos

text

Alias
UMLS CUI [1]
C0373706
Prolactin 2 - Prolactin - Result
Descripción

Prolactin measurement, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0373706
UMLS CUI [1,2]
C1274040
Neuro Assessment
Descripción

Neuro Assessment

Alias
UMLS CUI-1
C0027763
UMLS CUI-2
C0220825
Date and time of assessment
Descripción

Nervous system structure, Evaluation, Date in time, Time

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C0027763
UMLS CUI [1,2]
C0220825
UMLS CUI [1,3]
C0011008
UMLS CUI [1,4]
C0040223
Result
Descripción

Nervous system structure, Evaluation, Result

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0027763
UMLS CUI [1,2]
C0220825
UMLS CUI [1,3]
C1274040
Eye Examination
Descripción

Eye Examination

Alias
UMLS CUI-1
C0200149
Date and time of assessment
Descripción

Ophthalmic examination and evaluation, Date in time, Time

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0011008
UMLS CUI [1,3]
C0040223
Best-corrected ETDRS visual acuity right eye
Descripción

Ophthalmic examination and evaluation, ETDRS visual acuity chart, Right eye

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C1275992
UMLS CUI [1,3]
C0229089
Best-corrected ETDRS visual acuity right eye
Descripción

Ophthalmic examination and evaluation, ETDRS visual acuity chart, Right eye

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C1275992
UMLS CUI [1,3]
C0229089
Color vision right eye
Descripción

Ophthalmic examination and evaluation, Color Assessment, Right eye

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C1880121
UMLS CUI [1,3]
C0229089
Color vision right eye - Specify
Descripción

Ophthalmic examination and evaluation, Color Assessment, Right eye

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C1880121
UMLS CUI [1,3]
C0229089
Color vision left eye
Descripción

Ophthalmic examination and evaluation, Color Assessment, Left eye structure

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C1880121
UMLS CUI [1,3]
C0229090
Color vision left eye - Specify
Descripción

Ophthalmic examination and evaluation, Color Assessment, Left eye structure

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C1880121
UMLS CUI [1,3]
C0229090
Amsel grid - Right eye
Descripción

Ophthalmic examination and evaluation, Amsel chart, Right eye

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0491832
UMLS CUI [1,3]
C0229089
Amsel grid - Right eye - Specify
Descripción

Ophthalmic examination and evaluation, Amsel chart, Right eye

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0491832
UMLS CUI [1,3]
C0229089
Amsel grid - Left eye
Descripción

Ophthalmic examination and evaluation, Amsel chart, Left eye structure

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0491832
UMLS CUI [1,3]
C0229090
Amsel grid - Left eye - Specify
Descripción

Ophthalmic examination and evaluation, Amsel chart, Left eye structure

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0491832
UMLS CUI [1,3]
C0229090
External examination right eye
Descripción

Ophthalmic examination and evaluation, Examination of external eye, Right eye

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C2228438
UMLS CUI [1,3]
C0229089
External examination right eye - Specify
Descripción

Ophthalmic examination and evaluation, Examination of external eye, Right eye

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C2228438
UMLS CUI [1,3]
C0229089
External examination left eye
Descripción

Ophthalmic examination and evaluation, Examination of external eye, Left eye structure

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C2228438
UMLS CUI [1,3]
C0229090
External examination left eye - Specify
Descripción

Ophthalmic examination and evaluation, Examination of external eye, Left eye structure

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C2228438
UMLS CUI [1,3]
C0229090
Slit lamp right eye
Descripción

Ophthalmic examination and evaluation, Slit lamp biomicroscopy (procedure), Right eye

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0419360
UMLS CUI [1,3]
C0229089
Slit lamp right eye - Specify
Descripción

Ophthalmic examination and evaluation, Slit lamp biomicroscopy (procedure), Right eye

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0419360
UMLS CUI [1,3]
C0229089
Slit lamp left eye
Descripción

Ophthalmic examination and evaluation, Slit lamp biomicroscopy (procedure), Left eye structure

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0419360
UMLS CUI [1,3]
C0229090
Slit lamp left eye - Specify
Descripción

Ophthalmic examination and evaluation, Slit lamp biomicroscopy (procedure), Left eye structure

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0419360
UMLS CUI [1,3]
C0229090
Intraocular pressure right eye
Descripción

Ophthalmic examination and evaluation, Intraocular pressure finding, Right eye

Tipo de datos

integer

Unidades de medida
  • mmHg
Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0578862
UMLS CUI [1,3]
C0229089
mmHg
Intraocular pressure left eye
Descripción

Ophthalmic examination and evaluation, Intraocular pressure finding, Left eye structure

Tipo de datos

integer

Unidades de medida
  • mmHg
Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0578862
UMLS CUI [1,3]
C0229090
mmHg
Fundus examination posterior pole right eye
Descripción

Ophthalmic examination and evaluation, Fundus, Posterior pole, Right eye

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0740422
UMLS CUI [1,3]
C0444576
UMLS CUI [1,4]
C0229089
Fundus examination posterior pole right eye - Specify
Descripción

Ophthalmic examination and evaluation, Fundus, Posterior pole, Right eye

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0740422
UMLS CUI [1,3]
C0444576
UMLS CUI [1,4]
C0229089
Fundus examination posterior pole left eye
Descripción

Ophthalmic examination and evaluation, Fundus, Posterior pole, Left eye structure

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0740422
UMLS CUI [1,3]
C0444576
UMLS CUI [1,4]
C0229090
Fundus examination posterior pole left eye - Specify
Descripción

Ophthalmic examination and evaluation, Fundus, Posterior pole, Left eye structure

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0740422
UMLS CUI [1,3]
C0444576
UMLS CUI [1,4]
C0229090
Fundus examination periphery right eye
Descripción

Ophthalmic examination and evaluation, Fundus, Peripheral, Right eye

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0740422
UMLS CUI [1,3]
C0205100
UMLS CUI [1,4]
C0229089
Fundus examination periphery right eye - Specify
Descripción

Ophthalmic examination and evaluation, Fundus, Peripheral, Right eye

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0740422
UMLS CUI [1,3]
C0205100
UMLS CUI [1,4]
C0229089
Fundus examination periphery left eye
Descripción

Ophthalmic examination and evaluation, Fundus, Peripheral, Left eye structure

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0740422
UMLS CUI [1,3]
C0205100
UMLS CUI [1,4]
C0229090
Fundus examination periphery left eye - Specify
Descripción

Ophthalmic examination and evaluation, Fundus, Peripheral, Left eye structure

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0740422
UMLS CUI [1,3]
C0205100
UMLS CUI [1,4]
C0229090
Fundus examination blood vessel right eye
Descripción

Ophthalmic examination and evaluation, Fundus, Blood Vessel, Right eye

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0740422
UMLS CUI [1,3]
C0005847
UMLS CUI [1,4]
C0229089
Fundus examination blood vessel right eye - Specify
Descripción

Ophthalmic examination and evaluation, Fundus, Blood Vessel, Right eye

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0740422
UMLS CUI [1,3]
C0005847
UMLS CUI [1,4]
C0229089
Fundus examination blood vessel left eye
Descripción

Ophthalmic examination and evaluation, Fundus, Blood Vessel, Left eye structure

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0740422
UMLS CUI [1,3]
C0005847
UMLS CUI [1,4]
C0229090
Fundus examination blood vessel left eye - Specify
Descripción

Ophthalmic examination and evaluation, Fundus, Blood Vessel, Left eye structure

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0740422
UMLS CUI [1,3]
C0005847
UMLS CUI [1,4]
C0229090
Fundus examination optic disc right eye
Descripción

Ophthalmic examination and evaluation, Fundus, Optic Disk, Right eye

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0740422
UMLS CUI [1,3]
C0029127
UMLS CUI [1,4]
C0229089
Fundus examination optic disc right eye - Specify
Descripción

Ophthalmic examination and evaluation, Fundus, Optic Disk, Right eye

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0740422
UMLS CUI [1,3]
C0029127
UMLS CUI [1,4]
C0229089
Fundus examination optic disc left eye
Descripción

Ophthalmic examination and evaluation, Fundus, Optic Disk, Left eye structure

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0740422
UMLS CUI [1,3]
C0029127
UMLS CUI [1,4]
C0229090
Fundus examination optic disc left eye - Specify
Descripción

Ophthalmic examination and evaluation, Fundus, Optic Disk, Left eye structure

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0740422
UMLS CUI [1,3]
C0029127
UMLS CUI [1,4]
C0229090
ELT
Descripción

ELT

Alias
UMLS CUI-1
C0013746
UMLS CUI-2
C0242465
UMLS CUI-3
C0040223
UMLS CUI-4
C0442122
Reported ELT
Descripción

Ejaculation, Response Latency, Time, Reported

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0013746
UMLS CUI [1,2]
C0242465
UMLS CUI [1,3]
C0040223
UMLS CUI [1,4]
C0684224
Date of ELT
Descripción

Ejaculation, Response Latency, Time, Date in time

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0013746
UMLS CUI [1,2]
C0242465
UMLS CUI [1,3]
C0040223
UMLS CUI [1,4]
C0011008
ELT Baseline
Descripción

Ejaculation, Response Latency, Time, Baseline

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0013746
UMLS CUI [1,2]
C0242465
UMLS CUI [1,3]
C0040223
UMLS CUI [1,4]
C1442488
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Similar models

Screen

1 formularios
  1. StudyEvent: ODM
    1. Screen
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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)
Gender, Age
Item
Male between 18 and 50 years of age.
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Body Weight; Body mass index
Item
Body weight ≥ 50 kg (110 lbs) and BMI within the range 19.0 – 29.9 kg/m2 inclusive).
boolean
C0005910 (UMLS CUI [1])
C1305855 (UMLS CUI [2])
Heterosexuality
Item
Heterosexual orientation
boolean
C0019421 (UMLS CUI [1])
Premature Ejaculation, Symptoms
Item
Long term symptoms of PE that meet DSM-IV-TR criteria for PE: a. Persistent or recurrent ejaculation with minimal sexual stimulation before, on or shortly after penetration and before the person wishes it. The clinician must take into account factors that affect duration of the excitement phase, such as age, novelty of the sexual partner or situation, and recent frequency of sexual activity. b. The disturbance causes marked distress or interpersonal difficulty. c. The premature ejaculation is not due exclusively to the direct effects of a substance (e.g., withdrawal from opioids).
boolean
C0033038 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
Premature Ejaculation, Primary disorders
Item
Premature ejaculation is not due to any other concomitant medical condition
boolean
C0033038 (UMLS CUI [1,1])
C0277554 (UMLS CUI [1,2])
Premature Ejaculation
Item
Self-reported moderate or severe primary PE prior to screening with ejaculation occurring on or before penetration, or shortly there after with minimal stimulation.
boolean
C0033038 (UMLS CUI [1])
Premature Ejaculation, Response Latency, Time
Item
The patient has a baseline ELT less than 3 minutes.
boolean
C0033038 (UMLS CUI [1,1])
C0242465 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
Contraceptive methods
Item
Subjects must agree to use one of the contraception methods listed in Section 8.1. This criterion must be followed from the time of the first dose of study medication until 3 months after last dose.
boolean
C0700589 (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])
Ophthalmic examination and evaluation, Cooperation
Item
The subject is able to cooperate in all part of the eye examination (including dilation with mydriatics).
boolean
C0200149 (UMLS CUI [1,1])
C0392337 (UMLS CUI [1,2])
Visual Acuity
Item
The subject has a visual acuity that is equivalent to 20/30 in each eye, with appropriate correction if needed.
boolean
C0042812 (UMLS CUI [1])
QTcB - Bazett's Correction Formula; QTcF - Fridericia's Correction Formula
Item
QTcB o rQTcF < 450 msec.
boolean
C1882512 (UMLS CUI [1])
C1882513 (UMLS CUI [2])
Item Group
Exclusion Criteria
C0680251 (UMLS CUI-1)
Erectile dysfunction
Item
Erectile dysfunction. Erectile Function domain of International Index of Erectile Function questionnaire < 26.
boolean
C0242350 (UMLS CUI [1])
Other medical condition
Item
Any clinically relevant abnormality identified on the screening examination or any other medical condition or circumstance making the volunteer unsuitable for participation in the study.
boolean
C3843040 (UMLS CUI [1])
Migraine Disorders, Medical History
Item
The subject has a history of migraine.
boolean
C0149931 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
Mental disorders, Medical History
Item
The subject has a history of psychiatric illness, except for those symptoms related to their PE.
boolean
C0004936 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
Suicidal behavior, Medical History; Suicide attempt, Medical History
Item
Any history of suicidal attempts or behaviour.
boolean
C1760428 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
C0038663 (UMLS CUI [2,1])
C0262926 (UMLS CUI [2,2])
Disorder of eye, Medical History; Color blindness
Item
The subject has a history of any eye disorder or is colour blind, excluding myopia and presbyopia.
boolean
C0015397 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
C0242225 (UMLS CUI [2])
Long QT Syndrome; Cardiac conduction abnormality; Heart Diseases
Item
History of long QT syndrome (personal or family) or other cardiac conduction disorder, or other clinically significant cardiac disease.
boolean
C0023976 (UMLS CUI [1])
C1842820 (UMLS CUI [2])
C0018799 (UMLS CUI [3])
Hepatitis B surface antigen positive; Hepatitis C antibody positive
Item
A positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening (with the exception of phase I hepatic impairment studies, oncology studies, hepatitis, hepatic fibrosis, or HIV studies).
boolean
C0149709 (UMLS CUI [1])
C0281863 (UMLS CUI [2])
HIV antibody positive
Item
A positive test for HIV antibody.
boolean
C0920548 (UMLS CUI [1])
Medical History, Hypersensitivity, Drug intolerance
Item
History of sensitivity or intolerance to drugs that effect serotonin, including serotonin-reuptake inhibitors (SSRIs), or a history of drug or other allergy that, in the opinion of the investigator or GSK Medical Monitor, contraindicates their participation.
boolean
C0262926 (UMLS CUI [1,1])
C0020517 (UMLS CUI [1,2])
C0277585 (UMLS CUI [1,3])
Alcohol consumption
Item
History of regular alcohol consumption within 6 months of the study defined as: an average weekly intake of greater than 21 units or an average daily intake of greater than 3 units. One unit is equivalent to a half-pint (220mL) of beer or 1 (25ml) measure of spirits or 1 glass (125ml) of wine.
boolean
C0001948 (UMLS CUI [1])
Drug screen positive; Alcohol consumption screening, Positive Finding
Item
The subject has a positive pre-study drug/alcohol screen. A minimum list of drugs that will be screened for include amphetamines, barbiturates, cocaine, opiates, cannabinoids and benzodiazepines (can be repeated once at screening).
boolean
C0743295 (UMLS CUI [1])
C0420032 (UMLS CUI [2,1])
C1514241 (UMLS CUI [2,2])
Tobacco use
Item
Subject smokes more than 10 cigarettes per day.
boolean
C0543414 (UMLS CUI [1])
Red wine; Citrus aurantium; Grapefruit (food); GRAPEFRUIT JUICE
Item
Consumption of red wine, seville oranges, grapefruit or grapefruit juice [and/or pummelos, exotic citrus fruits, grapefruit hybrids] from 7 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])
Phosphodiesterase 5 inhibitor
Item
Regular use of any PDE-5 inhibitors.
boolean
C1318700 (UMLS CUI [1])
Premature Ejaculation, Therapeutic procedure
Item
Subject has received or is continuing to receive any treatment for PE (e.g.local anaesthetic spray, or intra-cavernosal injection) in the four weeks prior to the study start.
boolean
C0033038 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
Medication use, Vitamins, Herbal
Item
Use of prescription or non-prescription drugs, including vitamins, herbal and dietary supplements (including St John’s Wort) within 7 days (or 14 days if the drug is a potential enzyme inducer) or 5 half-lives (whichever is longer) prior to the first dose of study medication, unless in the opinion of the Investigator and GSK Medical Monitor the medication will not interfere with the study procedures or compromise subject safety.
boolean
C0013227 (UMLS CUI [1])
C0042890 (UMLS CUI [2])
C1504473 (UMLS CUI [3])
C0242295 (UMLS CUI [4])
Study Subject Participation Status
Item
The subject has participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer).
boolean
C2348568 (UMLS CUI [1])
Investigational New Drugs
Item
Exposure to more than four new chemical entities within 12 months prior to the first dosing day.
boolean
C0013230 (UMLS CUI [1])
Blood Donation
Item
Where participation in the study would result in donation of blood or blood products in excess of 500 mL within a 56 day period.
boolean
C0005794 (UMLS CUI [1])
Protocol Compliance
Item
Unwillingness or inability to follow the procedures outlined in the protocol.
boolean
C0525058 (UMLS CUI [1])
Item Group
Subject Identification
C2348585 (UMLS CUI-1)
Clinical Trial Subject Unique Identifier
Item
Subject number
integer
C2348585 (UMLS CUI [1])
Item Group
Vital Signs
C0518766 (UMLS CUI-1)
Vital signs, Semi-erect, Date in time, Time
Item
Semi-supine - Actual date/time
datetime
C0518766 (UMLS CUI [1,1])
C0522019 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
Body Height
Item
Height
integer
C0005890 (UMLS CUI [1])
Body Weight
Item
Weight
float
C0005910 (UMLS CUI [1])
Body mass index
Item
Body mass index
float
C1305855 (UMLS CUI [1])
Systolic Pressure, Semi-erect
Item
Semi-supine - Blood pressure - Systolic
integer
C0871470 (UMLS CUI [1,1])
C0522019 (UMLS CUI [1,2])
Diastolic blood pressure, Semi-erect
Item
Semi-supine - Blood pressure - Diastolic
integer
C0428883 (UMLS CUI [1,1])
C0522019 (UMLS CUI [1,2])
Heart rate, Semi-erect
Item
Semi-supine - Heart rate
integer
C0018810 (UMLS CUI [1,1])
C0522019 (UMLS CUI [1,2])
Respiratory rate, Semi-erect
Item
Semi-supine - Respiration rate
integer
C0231832 (UMLS CUI [1,1])
C0522019 (UMLS CUI [1,2])
Vital signs, Erect, Date in time, Time
Item
Standing - Actual date/time
datetime
C0518766 (UMLS CUI [1,1])
C0522014 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
Systolic Pressure, Erect
Item
Standing - Blood pressure - Systolic
integer
C0871470 (UMLS CUI [1,1])
C0522014 (UMLS CUI [1,2])
Diastolic blood pressure, Erect
Item
Standing - Blood pressure - Diastolic
integer
C0428883 (UMLS CUI [1,1])
C0522014 (UMLS CUI [1,2])
Heart rate, Erect
Item
Standing - Heart rate
integer
C0018810 (UMLS CUI [1,1])
C0522014 (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
Method of QTc Calculation
text
C0430456 (UMLS CUI [1,1])
C0855331 (UMLS CUI [1,2])
C2911685 (UMLS CUI [1,3])
12 lead ECG, Electrocardiogram QT corrected interval, Evaluation Method
Code List
Method of QTc Calculation
CL Item
Machine (1)
CL Item
Manual (2)
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
Local Laboratory - Haematology
C0022885 (UMLS CUI-1)
C0474523 (UMLS CUI-2)
Hematology, Sampling, Date in time, Time
Item
Date and time sample taken
datetime
C0474523 (UMLS CUI [1,1])
C0870078 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (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
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Hematology finding, Hemoglobin, Result
Item
Haemoglobin - Result
text
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
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
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
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])
Item
MCV
text
C0474523 (UMLS CUI [1,1])
C1948043 (UMLS CUI [1,2])
Hematology finding, Erythrocyte Mean Corpuscular Volume Measurement
Code List
MCV
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Hematology finding, Erythrocyte Mean Corpuscular Volume Measurement, Result
Item
MCV - Result
text
C0474523 (UMLS CUI [1,1])
C1948043 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Item
MCH
text
C0474523 (UMLS CUI [1,1])
C0369183 (UMLS CUI [1,2])
Hematology finding, Erythrocyte Mean Corpuscular Hemoglobin Test
Code List
MCH
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Hematology finding, Erythrocyte Mean Corpuscular Hemoglobin Test, Result
Item
MCH - Result
text
C0474523 (UMLS CUI [1,1])
C0369183 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Item
MCHC
text
C0474523 (UMLS CUI [1,1])
C0474535 (UMLS CUI [1,2])
Hematology finding, Mean corpuscular hemoglobin concentration determination
Code List
MCHC
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Hematology finding, Mean corpuscular hemoglobin concentration determination, Result
Item
MCHC - Result
text
C0474523 (UMLS CUI [1,1])
C0474535 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Item
Platelets
text
C0474523 (UMLS CUI [1,1])
C0005821 (UMLS CUI [1,2])
Hematology finding, Blood Platelets
Code List
Platelets
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Hematology finding, Blood Platelets, Result
Item
Platelets - Result
text
C0474523 (UMLS CUI [1,1])
C0005821 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
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
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
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])
Item
Neutrophils
text
C0474523 (UMLS CUI [1,1])
C0948762 (UMLS CUI [1,2])
Hematology finding, Absolute neutrophil count
Code List
Neutrophils
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
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])
Item
Lymphocytes
text
C0474523 (UMLS CUI [1,1])
C0200635 (UMLS CUI [1,2])
Hematology finding, Lymphocyte Count measurement
Code List
Lymphocytes
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
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])
Item
Monocytes
text
C0474523 (UMLS CUI [1,1])
C0750880 (UMLS CUI [1,2])
Hematology finding, Monocyte count result
Code List
Monocytes
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
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])
Item
Eosinophils
text
C0474523 (UMLS CUI [1,1])
C0200638 (UMLS CUI [1,2])
Hematology finding, Eosinophil count procedure
Code List
Eosinophils
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
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])
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
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
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])
Item
Reticulocytes
text
C0474523 (UMLS CUI [1,1])
C0206161 (UMLS CUI [1,2])
Hematology finding, Reticulocyte count (procedure)
Code List
Reticulocytes
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Hematology finding, Reticulocyte count (procedure), Result
Item
Reticulocytes - Result
text
C0474523 (UMLS CUI [1,1])
C0206161 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Item Group
Local Laboratory - Clinical Chemistry
C0022885 (UMLS CUI-1)
C0008000 (UMLS CUI-2)
Chemistry, Clinical, Sampling, Date in time, Time
Item
Date and time sample taken
datetime
C0008000 (UMLS CUI [1,1])
C0870078 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
Item
Urea
text
C0008000 (UMLS CUI [1,1])
C0523961 (UMLS CUI [1,2])
Chemistry, Clinical, Urea measurement
Code List
Urea
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Chemistry, Clinical, Urea measurement, Result
Item
Urea - Result
text
C0008000 (UMLS CUI [1,1])
C0523961 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Item
Creatinine
text
C0008000 (UMLS CUI [1,1])
C0201975 (UMLS CUI [1,2])
Chemistry, Clinical, Creatinine measurement
Code List
Creatinine
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Chemistry, Clinical, Creatinine measurement, Result
Item
Creatinine - Result
text
C0008000 (UMLS CUI [1,1])
C0201975 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
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
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
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])
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
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
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])
Item
Calcium
text
C0008000 (UMLS CUI [1,1])
C0201925 (UMLS CUI [1,2])
Chemistry, Clinical, Calcium measurement
Code List
Calcium
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Chemistry, Clinical, Calcium measurement, Result
Item
Calcium - Result
text
C0008000 (UMLS CUI [1,1])
C0201925 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Item
Chloride
text
C0008000 (UMLS CUI [1,1])
C0201952 (UMLS CUI [1,2])
Chemistry, Clinical, Chloride measurement
Code List
Chloride
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Chemistry, Clinical, Chloride measurement, Result
Item
Chloride - Result
text
C0008000 (UMLS CUI [1,1])
C0201952 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Item
Potassium
text
C0008000 (UMLS CUI [1,1])
C0202194 (UMLS CUI [1,2])
Chemistry, Clinical, Potassium measurement
Code List
Potassium
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Chemistry, Clinical, Potassium measurement, Result
Item
Potassium - Result
text
C0008000 (UMLS CUI [1,1])
C0202194 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Item
Sodium
text
C0008000 (UMLS CUI [1,1])
C0337443 (UMLS CUI [1,2])
Chemistry, Clinical, Sodium measurement
Code List
Sodium
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Chemistry, Clinical, Sodium measurement, Result
Item
Sodium - Result
text
C0008000 (UMLS CUI [1,1])
C0337443 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Item
Uric Acid
text
C0008000 (UMLS CUI [1,1])
C0041980 (UMLS CUI [1,2])
Chemistry, Clinical, Uric Acid
Code List
Uric Acid
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Chemistry, Clinical, Uric Acid, Result
Item
Uric Acid - Result
text
C0008000 (UMLS CUI [1,1])
C0041980 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Item
Glucose
text
C0008000 (UMLS CUI [1,1])
C0337438 (UMLS CUI [1,2])
Chemistry, Clinical, Glucose measurement
Code List
Glucose
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Chemistry, Clinical, Glucose measurement, Result
Item
Glucose - Result
text
C0008000 (UMLS CUI [1,1])
C0337438 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Item
Albumin
text
C0008000 (UMLS CUI [1,1])
C0201838 (UMLS CUI [1,2])
Chemistry, Clinical, Albumin measurement
Code List
Albumin
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Chemistry, Clinical, Albumin measurement, Result
Item
Albumin - Result
text
C0008000 (UMLS CUI [1,1])
C0201838 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Item
Total Protein
text
C0008000 (UMLS CUI [1,1])
C0555903 (UMLS CUI [1,2])
Chemistry, Clinical, Total protein measurement
Code List
Total Protein
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Chemistry, Clinical, Total protein measurement, Result
Item
Total Protein - Result
text
C0008000 (UMLS CUI [1,1])
C0555903 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Item
AST
text
C0008000 (UMLS CUI [1,1])
C0201899 (UMLS CUI [1,2])
Chemistry, Clinical, Aspartate aminotransferase measurement
Code List
AST
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
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])
Item
ALT
text
C0008000 (UMLS CUI [1,1])
C0201836 (UMLS CUI [1,2])
Chemistry, Clinical, Alanine aminotransferase measurement
Code List
ALT
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
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])
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
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
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])
Item Group
Local Laboratory - Urinalysis
C0022885 (UMLS CUI-1)
C0042014 (UMLS CUI-2)
Urinalysis, Sampling, Date in time, Time
Item
Date and time sample taken
datetime
C0042014 (UMLS CUI [1,1])
C0870078 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
Item
Result of dipstick
text
C0042014 (UMLS CUI [1,1])
C0430370 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Urinalysis, Urine dipstick test, Result
Code List
Result of dipstick
CL Item
No result (1)
CL Item
Negative (2)
CL Item
Positive (3)
Urinalysis, Urine Sediment Analysis Measurement
Item
Was a sedimentary microscopy performed?
boolean
C0430397 (UMLS CUI [1,1])
C2700128 (UMLS CUI [1,2])
Item
pH
text
C0042014 (UMLS CUI [1,1])
C0430370 (UMLS CUI [1,2])
C0042044 (UMLS CUI [1,3])
Urinalysis, Urine dipstick test, Urine pH measurement
Code List
pH
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Urinalysis, Urine dipstick test, Urine pH measurement, Result
Item
pH - Result
text
C0042014 (UMLS CUI [1,1])
C0430370 (UMLS CUI [1,2])
C0042044 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
Item
Glucose
text
C0042014 (UMLS CUI [1,1])
C0430370 (UMLS CUI [1,2])
C0004076 (UMLS CUI [1,3])
Urinalysis, Urine dipstick test, Glucose measurement
Code List
Glucose
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Urinalysis, Urine dipstick test, Glucose measurement, Result
Item
Glucose - Result
text
C0042014 (UMLS CUI [1,1])
C0430370 (UMLS CUI [1,2])
C0004076 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
Item
Protein
text
C0042014 (UMLS CUI [1,1])
C0430370 (UMLS CUI [1,2])
C0262923 (UMLS CUI [1,3])
Urinalysis, Urine dipstick test, Urine protein test
Code List
Protein
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Urinalysis, Urine dipstick test, Urine protein test, Result
Item
Protein - Result
text
C0042014 (UMLS CUI [1,1])
C0430370 (UMLS CUI [1,2])
C0262923 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
Item
Blood
text
C0042014 (UMLS CUI [1,1])
C0430370 (UMLS CUI [1,2])
C0430372 (UMLS CUI [1,3])
Urinalysis, Urine dipstick test, Urine dipstick for blood
Code List
Blood
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Urinalysis, Urine dipstick test, Urine dipstick for blood, Result
Item
Blood - Result
text
C0042014 (UMLS CUI [1,1])
C0430370 (UMLS CUI [1,2])
C0430372 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
Item
Ketones
text
C0042014 (UMLS CUI [1,1])
C0430370 (UMLS CUI [1,2])
C1991100 (UMLS CUI [1,3])
Urinalysis, Urine dipstick test, Ketones/Urine
Code List
Ketones
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Urinalysis, Urine dipstick test, Ketones/Urine, Result
Item
Ketones - Result
text
C0042014 (UMLS CUI [1,1])
C0430370 (UMLS CUI [1,2])
C1991100 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
Item
Specific Gravity
text
C0042014 (UMLS CUI [1,1])
C0430370 (UMLS CUI [1,2])
C0202517 (UMLS CUI [1,3])
Urinalysis, Urine dipstick test, Specific gravity measurement
Code List
Specific Gravity
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Urinalysis, Urine dipstick test, Specific gravity measurement, Result
Item
Specific Gravity - Result
text
C0042014 (UMLS CUI [1,1])
C0430370 (UMLS CUI [1,2])
C0202517 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
Urinalysis, Urine Sediment Analysis Measurement, Sampling, Date in time, Time
Item
Date and time sample taken (Sediment microscopy)
datetime
C0042014 (UMLS CUI [1,1])
C2700128 (UMLS CUI [1,2])
C0870078 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C0040223 (UMLS CUI [1,5])
Item
White blood cells
text
C0430397 (UMLS CUI [1,1])
C2700128 (UMLS CUI [1,2])
C0023508 (UMLS CUI [1,3])
Urinalysis, Urine Sediment Analysis Measurement, White Blood Cell Count procedure
Code List
White blood cells
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Urinalysis, Urine Sediment Analysis Measurement, White Blood Cell Count procedure, Result
Item
White blood cells - Result
text
C0430397 (UMLS CUI [1,1])
C2700128 (UMLS CUI [1,2])
C0023508 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
Item
Red blood cells
text
C0430397 (UMLS CUI [1,1])
C2700128 (UMLS CUI [1,2])
C0014772 (UMLS CUI [1,3])
Urinalysis, Urine Sediment Analysis Measurement, Red Blood Cell Count measurement
Code List
Red blood cells
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Urinalysis, Urine Sediment Analysis Measurement, Red Blood Cell Count measurement, Result
Item
Red blood cells - Result
text
C0430397 (UMLS CUI [1,1])
C2700128 (UMLS CUI [1,2])
C0014772 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
Item
Hyaline casts
text
C0430397 (UMLS CUI [1,1])
C2700128 (UMLS CUI [1,2])
C1254537 (UMLS CUI [1,3])
Urinalysis, Urine Sediment Analysis Measurement, Urine Hyaline Cast Test
Code List
Hyaline casts
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Urinalysis, Urine Sediment Analysis Measurement, Urine Hyaline Cast Test, Result
Item
Hyaline casts - Result
text
C0430397 (UMLS CUI [1,1])
C2700128 (UMLS CUI [1,2])
C1254537 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
Item
Cellular casts
text
C0430397 (UMLS CUI [1,1])
C2700128 (UMLS CUI [1,2])
C2699157 (UMLS CUI [1,3])
Urinalysis, Urine Sediment Analysis Measurement, Cellular Cast Measurement
Code List
Cellular casts
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Urinalysis, Urine Sediment Analysis Measurement, Cellular Cast Measurement, Result
Item
Cellular casts - Result
text
C0430397 (UMLS CUI [1,1])
C2700128 (UMLS CUI [1,2])
C2699157 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
Item Group
Local Laboratory - Hormones
C0022885 (UMLS CUI-1)
C0019932 (UMLS CUI-2)
Laboratory Procedures, Hormones, Sampling, Date in time, Time
Item
Date and time sample taken
datetime
C0022885 (UMLS CUI [1,1])
C0019932 (UMLS CUI [1,2])
C0870078 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C0040223 (UMLS CUI [1,5])
Item
Total Testosterone
text
C0022885 (UMLS CUI [1,1])
C0019932 (UMLS CUI [1,2])
C0202227 (UMLS CUI [1,3])
Laboratory Procedures, Hormones, Total Testosterone Measurement
Code List
Total Testosterone
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Laboratory Procedures, Hormones, Total Testosterone Measurement, Result
Item
Total Testosterone - Result
text
C0022885 (UMLS CUI [1,1])
C0019932 (UMLS CUI [1,2])
C0202227 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
Item
LH
text
C0022885 (UMLS CUI [1,1])
C0019932 (UMLS CUI [1,2])
C0202123 (UMLS CUI [1,3])
Laboratory Procedures, Hormones, Luteinizing hormone measurement
Code List
LH
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Laboratory Procedures, Hormones, Luteinizing hormone measurement, Result
Item
LH - Result
text
C0022885 (UMLS CUI [1,1])
C0019932 (UMLS CUI [1,2])
C0202123 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
Item
FSH
text
C0022885 (UMLS CUI [1,1])
C0019932 (UMLS CUI [1,2])
C0202022 (UMLS CUI [1,3])
Laboratory Procedures, Hormones, Follicle stimulating hormone measurement
Code List
FSH
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Laboratory Procedures, Hormones, Follicle stimulating hormone measurement, Result
Item
FSH - Result
text
C0022885 (UMLS CUI [1,1])
C0019932 (UMLS CUI [1,2])
C0202022 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
Item Group
Local Laboratory - FTEST
C0022885 (UMLS CUI-1)
C0202228 (UMLS CUI-2)
Free Testosterone Measurement, Sampling, Date in time, Time
Item
Date and time sample taken
datetime
C0202228 (UMLS CUI [1,1])
C0870078 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
Item
Free Testosterone
text
C0202228 (UMLS CUI [1])
Free Testosterone Measurement
Code List
Free Testosterone
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Free Testosterone Measurement, Result
Item
Free Testosterone - Result
text
C0202228 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
Item Group
Local Laboratory - Prolactin
C0022885 (UMLS CUI-1)
C0373706 (UMLS CUI-2)
Prolactin measurement, Sampling, Date in time, Time
Item
Prolactin 1 - Date and time sample taken
datetime
C0373706 (UMLS CUI [1,1])
C0870078 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
Item
Prolactin 1 - Prolactin
text
C0373706 (UMLS CUI [1])
Prolactin measurement
Code List
Prolactin 1 - Prolactin
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Prolactin measurement, Result
Item
Prolactin 1 - Prolactin - Result
text
C0373706 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
Prolactin measurement, Sampling, Date in time, Time
Item
Prolactin 2 - Date and time sample taken
datetime
C0373706 (UMLS CUI [1,1])
C0870078 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
Item
Prolactin 2 - Prolactin
text
C0373706 (UMLS CUI [1])
Prolactin measurement
Code List
Prolactin 2 - Prolactin
CL Item
Numeric result (1)
CL Item
Character result (2)
CL Item
No result (3)
Prolactin measurement, Result
Item
Prolactin 2 - Prolactin - Result
text
C0373706 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
Item Group
Neuro Assessment
C0027763 (UMLS CUI-1)
C0220825 (UMLS CUI-2)
Nervous system structure, Evaluation, Date in time, Time
Item
Date and time of assessment
datetime
C0027763 (UMLS CUI [1,1])
C0220825 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
Item
Result
text
C0027763 (UMLS CUI [1,1])
C0220825 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Nervous system structure, Evaluation, Result
Code List
Result
CL Item
Normal (1)
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
Item Group
Eye Examination
C0200149 (UMLS CUI-1)
Ophthalmic examination and evaluation, Date in time, Time
Item
Date and time of assessment
datetime
C0200149 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
Ophthalmic examination and evaluation, ETDRS visual acuity chart, Right eye
Item
Best-corrected ETDRS visual acuity right eye
text
C0200149 (UMLS CUI [1,1])
C1275992 (UMLS CUI [1,2])
C0229089 (UMLS CUI [1,3])
Ophthalmic examination and evaluation, ETDRS visual acuity chart, Right eye
Item
Best-corrected ETDRS visual acuity right eye
text
C0200149 (UMLS CUI [1,1])
C1275992 (UMLS CUI [1,2])
C0229089 (UMLS CUI [1,3])
Item
Color vision right eye
text
C0200149 (UMLS CUI [1,1])
C1880121 (UMLS CUI [1,2])
C0229089 (UMLS CUI [1,3])
Ophthalmic examination and evaluation, Color Assessment, Right eye
Code List
Color vision right eye
CL Item
Normal (1)
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
Item
Color vision right eye - Specify
text
C0200149 (UMLS CUI [1,1])
C1880121 (UMLS CUI [1,2])
C0229089 (UMLS CUI [1,3])
Ophthalmic examination and evaluation, Color Assessment, Right eye
Code List
Color vision right eye - Specify
Item
Color vision left eye
text
C0200149 (UMLS CUI [1,1])
C1880121 (UMLS CUI [1,2])
C0229090 (UMLS CUI [1,3])
Ophthalmic examination and evaluation, Color Assessment, Right eye
Code List
Color vision left eye
CL Item
Normal (1)
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
Item
Color vision left eye - Specify
text
C0200149 (UMLS CUI [1,1])
C1880121 (UMLS CUI [1,2])
C0229090 (UMLS CUI [1,3])
Ophthalmic examination and evaluation, Color Assessment, Right eye
Code List
Color vision left eye - Specify
Item
Amsel grid - Right eye
text
C0200149 (UMLS CUI [1,1])
C0491832 (UMLS CUI [1,2])
C0229089 (UMLS CUI [1,3])
Ophthalmic examination and evaluation, Color Assessment, Right eye
Code List
Amsel grid - Right eye
CL Item
Normal (1)
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
Ophthalmic examination and evaluation, Amsel chart, Right eye
Item
Amsel grid - Right eye - Specify
text
C0200149 (UMLS CUI [1,1])
C0491832 (UMLS CUI [1,2])
C0229089 (UMLS CUI [1,3])
Item
Amsel grid - Left eye
text
C0200149 (UMLS CUI [1,1])
C0491832 (UMLS CUI [1,2])
C0229090 (UMLS CUI [1,3])
Ophthalmic examination and evaluation, Color Assessment, Right eye
Code List
Amsel grid - Left eye
CL Item
Normal (1)
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
Ophthalmic examination and evaluation, Amsel chart, Left eye structure
Item
Amsel grid - Left eye - Specify
text
C0200149 (UMLS CUI [1,1])
C0491832 (UMLS CUI [1,2])
C0229090 (UMLS CUI [1,3])
Item
External examination right eye
text
C0200149 (UMLS CUI [1,1])
C2228438 (UMLS CUI [1,2])
C0229089 (UMLS CUI [1,3])
Ophthalmic examination and evaluation, Color Assessment, Right eye
Code List
External examination right eye
CL Item
Normal (1)
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
Item
External examination right eye - Specify
text
C0200149 (UMLS CUI [1,1])
C2228438 (UMLS CUI [1,2])
C0229089 (UMLS CUI [1,3])
Ophthalmic examination and evaluation, Color Assessment, Right eye
Code List
External examination right eye - Specify
Item
External examination left eye
text
C0200149 (UMLS CUI [1,1])
C2228438 (UMLS CUI [1,2])
C0229090 (UMLS CUI [1,3])
Ophthalmic examination and evaluation, Color Assessment, Right eye
Code List
External examination left eye
CL Item
Normal (1)
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
Item
External examination left eye - Specify
text
C0200149 (UMLS CUI [1,1])
C2228438 (UMLS CUI [1,2])
C0229090 (UMLS CUI [1,3])
Ophthalmic examination and evaluation, Color Assessment, Right eye
Code List
External examination left eye - Specify
Item
Slit lamp right eye
text
C0200149 (UMLS CUI [1,1])
C0419360 (UMLS CUI [1,2])
C0229089 (UMLS CUI [1,3])
Ophthalmic examination and evaluation, Slit lamp biomicroscopy (procedure), Right eye
Code List
Slit lamp right eye
CL Item
Normal (1)
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
Ophthalmic examination and evaluation, Slit lamp biomicroscopy (procedure), Right eye
Item
Slit lamp right eye - Specify
text
C0200149 (UMLS CUI [1,1])
C0419360 (UMLS CUI [1,2])
C0229089 (UMLS CUI [1,3])
Item
Slit lamp left eye
text
C0200149 (UMLS CUI [1,1])
C0419360 (UMLS CUI [1,2])
C0229090 (UMLS CUI [1,3])
Ophthalmic examination and evaluation, Color Assessment, Right eye
Code List
Slit lamp left eye
CL Item
Normal (1)
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
Ophthalmic examination and evaluation, Slit lamp biomicroscopy (procedure), Left eye structure
Item
Slit lamp left eye - Specify
text
C0200149 (UMLS CUI [1,1])
C0419360 (UMLS CUI [1,2])
C0229090 (UMLS CUI [1,3])
Ophthalmic examination and evaluation, Intraocular pressure finding, Right eye
Item
Intraocular pressure right eye
integer
C0200149 (UMLS CUI [1,1])
C0578862 (UMLS CUI [1,2])
C0229089 (UMLS CUI [1,3])
Ophthalmic examination and evaluation, Intraocular pressure finding, Left eye structure
Item
Intraocular pressure left eye
integer
C0200149 (UMLS CUI [1,1])
C0578862 (UMLS CUI [1,2])
C0229090 (UMLS CUI [1,3])
Item
Fundus examination posterior pole right eye
text
C0200149 (UMLS CUI [1,1])
C0740422 (UMLS CUI [1,2])
C0444576 (UMLS CUI [1,3])
C0229089 (UMLS CUI [1,4])
Ophthalmic examination and evaluation, Intraocular pressure finding, Right eye
Code List
Fundus examination posterior pole right eye
CL Item
Normal (1)
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
Item
Fundus examination posterior pole right eye - Specify
text
C0200149 (UMLS CUI [1,1])
C0740422 (UMLS CUI [1,2])
C0444576 (UMLS CUI [1,3])
C0229089 (UMLS CUI [1,4])
Ophthalmic examination and evaluation, Intraocular pressure finding, Right eye
Code List
Fundus examination posterior pole right eye - Specify
Item
Fundus examination posterior pole left eye
text
C0200149 (UMLS CUI [1,1])
C0740422 (UMLS CUI [1,2])
C0444576 (UMLS CUI [1,3])
C0229090 (UMLS CUI [1,4])
Ophthalmic examination and evaluation, Intraocular pressure finding, Right eye
Code List
Fundus examination posterior pole left eye
CL Item
Normal (1)
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
Ophthalmic examination and evaluation, Fundus, Posterior pole, Left eye structure
Item
Fundus examination posterior pole left eye - Specify
text
C0200149 (UMLS CUI [1,1])
C0740422 (UMLS CUI [1,2])
C0444576 (UMLS CUI [1,3])
C0229090 (UMLS CUI [1,4])
Item
Fundus examination periphery right eye
text
C0200149 (UMLS CUI [1,1])
C0740422 (UMLS CUI [1,2])
C0205100 (UMLS CUI [1,3])
C0229089 (UMLS CUI [1,4])
Ophthalmic examination and evaluation, Intraocular pressure finding, Right eye
Code List
Fundus examination periphery right eye
CL Item
Normal (1)
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
Ophthalmic examination and evaluation, Fundus, Peripheral, Right eye
Item
Fundus examination periphery right eye - Specify
text
C0200149 (UMLS CUI [1,1])
C0740422 (UMLS CUI [1,2])
C0205100 (UMLS CUI [1,3])
C0229089 (UMLS CUI [1,4])
Item
Fundus examination periphery left eye
text
C0200149 (UMLS CUI [1,1])
C0740422 (UMLS CUI [1,2])
C0205100 (UMLS CUI [1,3])
C0229090 (UMLS CUI [1,4])
Ophthalmic examination and evaluation, Intraocular pressure finding, Right eye
Code List
Fundus examination periphery left eye
CL Item
Normal (1)
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
Ophthalmic examination and evaluation, Fundus, Peripheral, Left eye structure
Item
Fundus examination periphery left eye - Specify
text
C0200149 (UMLS CUI [1,1])
C0740422 (UMLS CUI [1,2])
C0205100 (UMLS CUI [1,3])
C0229090 (UMLS CUI [1,4])
Item
Fundus examination blood vessel right eye
text
C0200149 (UMLS CUI [1,1])
C0740422 (UMLS CUI [1,2])
C0005847 (UMLS CUI [1,3])
C0229089 (UMLS CUI [1,4])
Ophthalmic examination and evaluation, Intraocular pressure finding, Right eye
Code List
Fundus examination blood vessel right eye
CL Item
Normal (1)
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
Item
Fundus examination blood vessel right eye - Specify
text
C0200149 (UMLS CUI [1,1])
C0740422 (UMLS CUI [1,2])
C0005847 (UMLS CUI [1,3])
C0229089 (UMLS CUI [1,4])
Ophthalmic examination and evaluation, Intraocular pressure finding, Right eye
Code List
Fundus examination blood vessel right eye - Specify
Item
Fundus examination blood vessel left eye
text
C0200149 (UMLS CUI [1,1])
C0740422 (UMLS CUI [1,2])
C0005847 (UMLS CUI [1,3])
C0229090 (UMLS CUI [1,4])
Ophthalmic examination and evaluation, Intraocular pressure finding, Right eye
Code List
Fundus examination blood vessel left eye
CL Item
Normal (1)
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
Item
Fundus examination blood vessel left eye - Specify
text
C0200149 (UMLS CUI [1,1])
C0740422 (UMLS CUI [1,2])
C0005847 (UMLS CUI [1,3])
C0229090 (UMLS CUI [1,4])
Ophthalmic examination and evaluation, Intraocular pressure finding, Right eye
Code List
Fundus examination blood vessel left eye - Specify
Item
Fundus examination optic disc right eye
text
C0200149 (UMLS CUI [1,1])
C0740422 (UMLS CUI [1,2])
C0029127 (UMLS CUI [1,3])
C0229089 (UMLS CUI [1,4])
Ophthalmic examination and evaluation, Intraocular pressure finding, Right eye
Code List
Fundus examination optic disc right eye
CL Item
Normal (1)
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
Item
Fundus examination optic disc right eye - Specify
text
C0200149 (UMLS CUI [1,1])
C0740422 (UMLS CUI [1,2])
C0029127 (UMLS CUI [1,3])
C0229089 (UMLS CUI [1,4])
Ophthalmic examination and evaluation, Intraocular pressure finding, Right eye
Code List
Fundus examination optic disc right eye - Specify
Item
Fundus examination optic disc left eye
text
C0200149 (UMLS CUI [1,1])
C0740422 (UMLS CUI [1,2])
C0029127 (UMLS CUI [1,3])
C0229090 (UMLS CUI [1,4])
Ophthalmic examination and evaluation, Intraocular pressure finding, Right eye
Code List
Fundus examination optic disc left eye
CL Item
Normal (1)
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
Ophthalmic examination and evaluation, Fundus, Optic Disk, Left eye structure
Item
Fundus examination optic disc left eye - Specify
text
C0200149 (UMLS CUI [1,1])
C0740422 (UMLS CUI [1,2])
C0029127 (UMLS CUI [1,3])
C0229090 (UMLS CUI [1,4])
Item Group
ELT
C0013746 (UMLS CUI-1)
C0242465 (UMLS CUI-2)
C0040223 (UMLS CUI-3)
C0442122 (UMLS CUI-4)
Ejaculation, Response Latency, Time, Reported
Item
Reported ELT
text
C0013746 (UMLS CUI [1,1])
C0242465 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
C0684224 (UMLS CUI [1,4])
Ejaculation, Response Latency, Time, Date in time
Item
Date of ELT
date
C0013746 (UMLS CUI [1,1])
C0242465 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
Ejaculation, Response Latency, Time, Baseline
Item
ELT Baseline
text
C0013746 (UMLS CUI [1,1])
C0242465 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
C1442488 (UMLS CUI [1,4])
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