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])
Clinical Trial Subject Unique Identifier
Item
Subject number
text
C2348585 (UMLS CUI [1])
Date of visit, Assessment Date
Item
Date of visit/assessment
date
C1320303 (UMLS CUI [1,1])
C2985720 (UMLS CUI [1,2])
Eligibility Determination
Item
Did the subject meet all the entry criteria?
boolean
C0013893 (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])
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])
Clinical Trial Subject Unique Identifier
Item
Subject number
integer
C2348585 (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])
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])
Code List
Method of QTc Calculation
Item
Result of the ECG
text
C0430456 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
Code List
Result of the ECG
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
CL Item
No result (not available) (4)
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])
CL Item
Numeric result (1)
CL Item
Character result (2)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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])
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)
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)
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])
Code List
Total Bilirubin
CL Item
Numeric result (1)
CL Item
Character result (2)
Chemistry, Clinical, Bilirubin, total measurement, Result
Item
Total Bilirubin - Result
text
C0008000 (UMLS CUI [1,1])
C0201913 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Item
Direct Bilirubin
text
C0008000 (UMLS CUI [1,1])
C0201916 (UMLS CUI [1,2])
Code List
Direct Bilirubin
CL Item
Numeric result (1)
CL Item
Character result (2)
Chemistry, Clinical, Bilirubin, direct measurement, Result
Item
Direct Bilirubin - Result
text
C0008000 (UMLS CUI [1,1])
C0201916 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Item
Calcium
text
C0008000 (UMLS CUI [1,1])
C0201925 (UMLS CUI [1,2])
CL Item
Numeric result (1)
CL Item
Character result (2)
Chemistry, Clinical, Calcium measurement, Result
Item
Calcium - Result
text
C0008000 (UMLS CUI [1,1])
C0201925 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Item
Chloride
text
C0008000 (UMLS CUI [1,1])
C0201952 (UMLS CUI [1,2])
CL Item
Numeric result (1)
CL Item
Character result (2)
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)
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)
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)
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)
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)
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)
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)
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)
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])
Code List
Alkaline Phosphatase
CL Item
Numeric result (1)
CL Item
Character result (2)
Chemistry, Clinical, Alkaline phosphatase measurement, Result
Item
Alkaline Phosphatase - Result
text
C0008000 (UMLS CUI [1,1])
C0201850 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
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
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)
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)
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)
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)
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)
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])
Code List
Specific Gravity
CL Item
Numeric result (1)
CL Item
Character result (2)
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])
Code List
White blood cells
CL Item
Numeric result (1)
CL Item
Character result (2)
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])
Code List
Red blood cells
CL Item
Numeric result (1)
CL Item
Character result (2)
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)
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)
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])
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])
Code List
Total Testosterone
CL Item
Numeric result (1)
CL Item
Character result (2)
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)
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)
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])
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)
Free Testosterone Measurement, Result
Item
Free Testosterone - Result
text
C0202228 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
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)
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)
Prolactin measurement, Result
Item
Prolactin 2 - Prolactin - Result
text
C0373706 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
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
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
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])
Code List
Color vision right eye
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])
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])
Code List
Color vision left eye
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])
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])
Code List
Amsel grid - Right eye
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])
Code List
Amsel grid - Left eye
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])
Code List
External examination right eye
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])
Code List
External examination left eye
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])
Code List
Slit lamp right eye
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])
Code List
Slit lamp left eye
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
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])
Code List
Fundus examination posterior pole left eye
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])
Code List
Fundus examination periphery right eye
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])
Code List
Fundus examination periphery left eye
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])
Code List
Fundus examination blood vessel right eye
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])
Code List
Fundus examination blood vessel left eye
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])
Code List
Fundus examination optic disc right eye
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])
Code List
Fundus examination optic disc left eye
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])
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])