ID

40893

Description

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

Mots-clés

  1. 31/05/2020 31/05/2020 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

31 mai 2020

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 4.0

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Effect of GSK958108 on ejaculatory latency time (ELT); NCT00861484

  1. StudyEvent: ODM
    1. Screen
Inform Screening
Description

Inform Screening

Alias
UMLS CUI-1
C0220908
Subject initials
Description

Clinical trial participant (person), Person Initials

Type de données

text

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

Patient date of birth

Type de données

date

Alias
UMLS CUI [1]
C0421451
Inform Enrollment
Description

Inform Enrollment

Alias
UMLS CUI-1
C1516879
Subject number
Description

Clinical Trial Subject Unique Identifier

Type de données

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

Type de données

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

Type de données

date

Alias
UMLS CUI [1]
C0421451
Sex
Description

Gender

Type de données

text

Alias
UMLS CUI [1]
C0079399
Ethnicity
Description

Ethnic group

Type de données

text

Alias
UMLS CUI [1]
C0015031
Geographic ancestry
Description

Your ancestry or national origin

Type de données

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

Type de données

boolean

Alias
UMLS CUI [1]
C0013893
Inclusion Criteria
Description

Inclusion Criteria

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

Gender, Age

Type de données

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).
Description

Body Weight; Body mass index

Type de données

boolean

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

Heterosexuality

Type de données

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).
Description

Premature Ejaculation, Symptoms

Type de données

boolean

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

Premature Ejaculation, Primary disorders

Type de données

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.
Description

Premature Ejaculation

Type de données

boolean

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

Premature Ejaculation, Response Latency, Time

Type de données

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.
Description

Contraceptive methods

Type de données

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.
Description

Informed Consent

Type de données

boolean

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

Ophthalmic examination and evaluation, Cooperation

Type de données

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.
Description

Visual Acuity

Type de données

boolean

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

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

Type de données

boolean

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

Exclusion Criteria

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

Erectile dysfunction

Type de données

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.
Description

Other medical condition

Type de données

boolean

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

Migraine Disorders, Medical History

Type de données

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.
Description

Mental disorders, Medical History

Type de données

boolean

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

Suicidal behavior, Medical History; Suicide attempt, Medical History

Type de données

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.
Description

Disorder of eye, Medical History; Color blindness

Type de données

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.
Description

Long QT Syndrome; Cardiac conduction abnormality; Heart Diseases

Type de données

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).
Description

Hepatitis B surface antigen positive; Hepatitis C antibody positive

Type de données

boolean

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

HIV antibody positive

Type de données

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.
Description

Medical History, Hypersensitivity, Drug intolerance

Type de données

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.
Description

Alcohol consumption

Type de données

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).
Description

Drug screen positive; Alcohol consumption screening, Positive Finding

Type de données

boolean

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

Tobacco use

Type de données

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.
Description

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

Type de données

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.
Description

Phosphodiesterase 5 inhibitor

Type de données

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.
Description

Premature Ejaculation, Therapeutic procedure

Type de données

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.
Description

Medication use, Vitamins, Herbal

Type de données

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).
Description

Study Subject Participation Status

Type de données

boolean

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

Investigational New Drugs

Type de données

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.
Description

Blood Donation

Type de données

boolean

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

Protocol Compliance

Type de données

boolean

Alias
UMLS CUI [1]
C0525058
Subject Identification
Description

Subject Identification

Alias
UMLS CUI-1
C2348585
Subject number
Description

Clinical Trial Subject Unique Identifier

Type de données

integer

Alias
UMLS CUI [1]
C2348585
Vital Signs
Description

Vital Signs

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

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

Type de données

datetime

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

Body Height

Type de données

integer

Unités de mesure
  • cm
Alias
UMLS CUI [1]
C0005890
cm
Weight
Description

Body Weight

Type de données

float

Unités de mesure
  • kg
Alias
UMLS CUI [1]
C0005910
kg
Body mass index
Description

Body mass index

Type de données

float

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

Systolic Pressure, Semi-erect

Type de données

integer

Unités de mesure
  • mmHg
Alias
UMLS CUI [1,1]
C0871470
UMLS CUI [1,2]
C0522019
mmHg
Semi-supine - Blood pressure - Diastolic
Description

Diastolic blood pressure, Semi-erect

Type de données

integer

Unités de mesure
  • mmHg
Alias
UMLS CUI [1,1]
C0428883
UMLS CUI [1,2]
C0522019
mmHg
Semi-supine - Heart rate
Description

Heart rate, Semi-erect

Type de données

integer

Unités de mesure
  • bpm
Alias
UMLS CUI [1,1]
C0018810
UMLS CUI [1,2]
C0522019
bpm
Semi-supine - Respiration rate
Description

Respiratory rate, Semi-erect

Type de données

integer

Unités de mesure
  • breaths/min
Alias
UMLS CUI [1,1]
C0231832
UMLS CUI [1,2]
C0522019
breaths/min
Standing - Actual date/time
Description

Vital signs, Erect, Date in time, Time

Type de données

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
Description

Systolic Pressure, Erect

Type de données

integer

Unités de mesure
  • mmHg
Alias
UMLS CUI [1,1]
C0871470
UMLS CUI [1,2]
C0522014
mmHg
Standing - Blood pressure - Diastolic
Description

Diastolic blood pressure, Erect

Type de données

integer

Unités de mesure
  • mmHg
Alias
UMLS CUI [1,1]
C0428883
UMLS CUI [1,2]
C0522014
mmHg
Standing - Heart rate
Description

Heart rate, Erect

Type de données

integer

Unités de mesure
  • bpm
Alias
UMLS CUI [1,1]
C0018810
UMLS CUI [1,2]
C0522014
bpm
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

Type de données

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

Type de données

integer

Unités de mesure
  • bpm
Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C0018810
bpm
PR Interval
Description

12 lead ECG, Electrocardiogram: P-R interval

Type de données

integer

Unités de mesure
  • msec
Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C0429087
msec
QRS Duration
Description

12 lead ECG, QRS complex duration

Type de données

integer

Unités de mesure
  • msec
Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C0429025
msec
Uncorrected QT Interval
Description

12 lead ECG, QT interval - finding

Type de données

integer

Unités de mesure
  • msec
Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C1287082
msec
QTc Interval
Description

12 lead ECG, Electrocardiogram QT corrected interval

Type de données

integer

Unités de mesure
  • msec
Alias
UMLS CUI [1,1]
C0430456
UMLS CUI [1,2]
C0855331
Method of QTc Calculation
Description

12 lead ECG, Electrocardiogram QT corrected interval, Evaluation Method

Type de données

text

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

12 lead ECG, Result

Type de données

text

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

Local Laboratory - Haematology

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

Hematology, Sampling, Date in time, Time

Type de données

datetime

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

Hematology finding, Hemoglobin

Type de données

text

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

Hematology finding, Hemoglobin, Result

Type de données

text

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

Hematology finding, Red Blood Cell Count measurement

Type de données

text

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

Hematology finding, Red Blood Cell Count measurement, Result

Type de données

text

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

Hematology finding, Erythrocyte Mean Corpuscular Volume Measurement

Type de données

text

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

Hematology finding, Erythrocyte Mean Corpuscular Volume Measurement, Result

Type de données

text

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

Hematology finding, Erythrocyte Mean Corpuscular Hemoglobin Test

Type de données

text

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

Hematology finding, Erythrocyte Mean Corpuscular Hemoglobin Test, Result

Type de données

text

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

Hematology finding, Mean corpuscular hemoglobin concentration determination

Type de données

text

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

Hematology finding, Mean corpuscular hemoglobin concentration determination, Result

Type de données

text

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

Hematology finding, Blood Platelets

Type de données

text

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

Hematology finding, Blood Platelets, Result

Type de données

text

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

Hematology finding, White Blood Cell Count procedure

Type de données

text

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

Hematology finding, White Blood Cell Count procedure, Result

Type de données

text

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

Hematology finding, Absolute neutrophil count

Type de données

text

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

Hematology finding, Absolute neutrophil count, Result

Type de données

text

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

Hematology finding, Lymphocyte Count measurement

Type de données

text

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

Hematology finding, Lymphocyte Count measurement, Result

Type de données

text

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

Hematology finding, Monocyte count result

Type de données

text

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

Hematology finding, Monocyte count result, Result

Type de données

text

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

Hematology finding, Eosinophil count procedure

Type de données

text

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

Hematology finding, Eosinophil count procedure, Result

Type de données

text

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

Hematology finding, Blood basophil count (lab test)

Type de données

text

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

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

Type de données

text

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

Hematology finding, Reticulocyte count (procedure)

Type de données

text

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

Hematology finding, Reticulocyte count (procedure), Result

Type de données

text

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

Local Laboratory - Clinical Chemistry

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

Chemistry, Clinical, Sampling, Date in time, Time

Type de données

datetime

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

Chemistry, Clinical, Urea measurement

Type de données

text

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

Chemistry, Clinical, Urea measurement, Result

Type de données

text

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

Chemistry, Clinical, Creatinine measurement

Type de données

text

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

Chemistry, Clinical, Creatinine measurement, Result

Type de données

text

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

Chemistry, Clinical, Bilirubin, total measurement

Type de données

text

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

Chemistry, Clinical, Bilirubin, total measurement, Result

Type de données

text

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

Chemistry, Clinical, Bilirubin, direct measurement

Type de données

text

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

Chemistry, Clinical, Bilirubin, direct measurement, Result

Type de données

text

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

Chemistry, Clinical, Calcium measurement

Type de données

text

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

Chemistry, Clinical, Calcium measurement, Result

Type de données

text

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

Chemistry, Clinical, Chloride measurement

Type de données

text

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

Chemistry, Clinical, Chloride measurement, Result

Type de données

text

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

Chemistry, Clinical, Potassium measurement

Type de données

text

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

Chemistry, Clinical, Potassium measurement, Result

Type de données

text

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

Chemistry, Clinical, Sodium measurement

Type de données

text

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

Chemistry, Clinical, Sodium measurement, Result

Type de données

text

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

Chemistry, Clinical, Uric Acid

Type de données

text

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

Chemistry, Clinical, Uric Acid, Result

Type de données

text

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

Chemistry, Clinical, Glucose measurement

Type de données

text

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

Chemistry, Clinical, Glucose measurement, Result

Type de données

text

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

Chemistry, Clinical, Albumin measurement

Type de données

text

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

Chemistry, Clinical, Albumin measurement, Result

Type de données

text

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

Chemistry, Clinical, Total protein measurement

Type de données

text

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

Chemistry, Clinical, Total protein measurement, Result

Type de données

text

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

Chemistry, Clinical, Aspartate aminotransferase measurement

Type de données

text

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

Chemistry, Clinical, Aspartate aminotransferase measurement, Result

Type de données

text

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

Chemistry, Clinical, Alanine aminotransferase measurement

Type de données

text

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

Chemistry, Clinical, Alanine aminotransferase measurement, Result

Type de données

text

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

Chemistry, Clinical, Alkaline phosphatase measurement

Type de données

text

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

Chemistry, Clinical, Alkaline phosphatase measurement, Result

Type de données

text

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

Local Laboratory - Urinalysis

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

Urinalysis, Sampling, Date in time, Time

Type de données

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
Description

Urinalysis, Urine dipstick test, Result

Type de données

text

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

Urinalysis, Urine Sediment Analysis Measurement

Type de données

boolean

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

Urinalysis, Urine dipstick test, Urine pH measurement

Type de données

text

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

Urinalysis, Urine dipstick test, Urine pH measurement, Result

Type de données

text

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

Urinalysis, Urine dipstick test, Glucose measurement

Type de données

text

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

Urinalysis, Urine dipstick test, Glucose measurement, Result

Type de données

text

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

Urinalysis, Urine dipstick test, Urine protein test

Type de données

text

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

Urinalysis, Urine dipstick test, Urine protein test, Result

Type de données

text

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

Urinalysis, Urine dipstick test, Urine dipstick for blood

Type de données

text

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

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

Type de données

text

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

Urinalysis, Urine dipstick test, Ketones/Urine

Type de données

text

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

Urinalysis, Urine dipstick test, Ketones/Urine, Result

Type de données

text

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

Urinalysis, Urine dipstick test, Specific gravity measurement

Type de données

text

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

Urinalysis, Urine dipstick test, Specific gravity measurement, Result

Type de données

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)
Description

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

Type de données

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
Description

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

Type de données

text

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

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

Type de données

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
Description

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

Type de données

text

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

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

Type de données

text

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

Urinalysis, Urine Sediment Analysis Measurement, Urine Hyaline Cast Test

Type de données

text

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

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

Type de données

text

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

Urinalysis, Urine Sediment Analysis Measurement, Cellular Cast Measurement

Type de données

text

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

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

Type de données

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
Description

Local Laboratory - Hormones

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

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

Type de données

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
Description

Laboratory Procedures, Hormones, Total Testosterone Measurement

Type de données

text

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

Laboratory Procedures, Hormones, Total Testosterone Measurement, Result

Type de données

text

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

Laboratory Procedures, Hormones, Luteinizing hormone measurement

Type de données

text

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

Laboratory Procedures, Hormones, Luteinizing hormone measurement, Result

Type de données

text

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

Laboratory Procedures, Hormones, Follicle stimulating hormone measurement

Type de données

text

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

Laboratory Procedures, Hormones, Follicle stimulating hormone measurement, Result

Type de données

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
Description

Local Laboratory - FTEST

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

Free Testosterone Measurement, Sampling, Date in time, Time

Type de données

datetime

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

Free Testosterone Measurement

Type de données

text

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

Free Testosterone Measurement, Result

Type de données

text

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

Local Laboratory - Prolactin

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

Prolactin measurement, Sampling, Date in time, Time

Type de données

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
Description

Prolactin measurement

Type de données

text

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

Prolactin measurement, Result

Type de données

text

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

Prolactin measurement, Sampling, Date in time, Time

Type de données

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
Description

Prolactin measurement

Type de données

text

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

Prolactin measurement, Result

Type de données

text

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

Neuro Assessment

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

Nervous system structure, Evaluation, Date in time, Time

Type de données

datetime

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

Nervous system structure, Evaluation, Result

Type de données

text

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

Eye Examination

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

Ophthalmic examination and evaluation, Date in time, Time

Type de données

datetime

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

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

Type de données

text

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

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

Type de données

text

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

Ophthalmic examination and evaluation, Color Assessment, Right eye

Type de données

text

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

Ophthalmic examination and evaluation, Color Assessment, Right eye

Type de données

text

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

Ophthalmic examination and evaluation, Color Assessment, Left eye structure

Type de données

text

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

Ophthalmic examination and evaluation, Color Assessment, Left eye structure

Type de données

text

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

Ophthalmic examination and evaluation, Amsel chart, Right eye

Type de données

text

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

Ophthalmic examination and evaluation, Amsel chart, Right eye

Type de données

text

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

Ophthalmic examination and evaluation, Amsel chart, Left eye structure

Type de données

text

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

Ophthalmic examination and evaluation, Amsel chart, Left eye structure

Type de données

text

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

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

Type de données

text

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

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

Type de données

text

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

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

Type de données

text

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

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

Type de données

text

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

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

Type de données

text

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

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

Type de données

text

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

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

Type de données

text

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

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

Type de données

text

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

Ophthalmic examination and evaluation, Intraocular pressure finding, Right eye

Type de données

integer

Unités de mesure
  • mmHg
Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0578862
UMLS CUI [1,3]
C0229089
mmHg
Intraocular pressure left eye
Description

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

Type de données

integer

Unités de mesure
  • mmHg
Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0578862
UMLS CUI [1,3]
C0229090
mmHg
Fundus examination posterior pole right eye
Description

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

Type de données

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
Description

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

Type de données

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
Description

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

Type de données

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
Description

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

Type de données

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
Description

Ophthalmic examination and evaluation, Fundus, Peripheral, Right eye

Type de données

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
Description

Ophthalmic examination and evaluation, Fundus, Peripheral, Right eye

Type de données

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
Description

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

Type de données

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
Description

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

Type de données

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
Description

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

Type de données

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
Description

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

Type de données

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
Description

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

Type de données

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
Description

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

Type de données

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
Description

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

Type de données

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
Description

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

Type de données

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
Description

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

Type de données

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
Description

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

Type de données

text

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

ELT

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

Ejaculation, Response Latency, Time, Reported

Type de données

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
Description

Ejaculation, Response Latency, Time, Date in time

Type de données

date

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

Ejaculation, Response Latency, Time, Baseline

Type de données

text

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

Similar models

  1. StudyEvent: ODM
    1. Screen
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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])
Code List
Sex
CL Item
Male (1)
Item
Ethnicity
text
C0015031 (UMLS CUI [1])
Code List
Ethnicity
CL Item
Hispanic or Latino (1)
CL Item
Not Hispanic or Latino (2)
Item
Geographic ancestry
text
C3841890 (UMLS CUI [1])
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])
Item
Method of QTc Calculation
text
C0430456 (UMLS CUI [1,1])
C0855331 (UMLS CUI [1,2])
C2911685 (UMLS CUI [1,3])
CL Item
Machine (1)
CL Item
Manual (2)
Item
Result of the ECG
text
C0430456 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
Item
Color vision left eye
text
C0200149 (UMLS CUI [1,1])
C1880121 (UMLS CUI [1,2])
C0229090 (UMLS CUI [1,3])
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])
Item
Amsel grid - Right eye
text
C0200149 (UMLS CUI [1,1])
C0491832 (UMLS CUI [1,2])
C0229089 (UMLS CUI [1,3])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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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