ID

21172

Beskrivning

Monotherapy Versus Placebo Over 14 or 17 Days in Healthy and Hepatitis C Infected Adults; ODM derived from: https://clinicaltrials.gov/show/NCT00439959

Länk

https://clinicaltrials.gov/show/NCT00439959

Nyckelord

  1. 2017-04-12 2017-04-12 -
Uppladdad den

12 april 2017

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Hepatitis C, Chronic NCT00439959

Eligibility Hepatitis C, Chronic NCT00439959

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
healthy males & females
Beskrivning

Gender and health status

Datatyp

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0018759
part 1 ages 18-60
Beskrivning

Age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
part 2 ages 18-50 & 65-80
Beskrivning

Age specification

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0001779
UMLS CUI [1,2]
C2348235
within normal weight range given your height
Beskrivning

Weight and height

Datatyp

boolean

Alias
UMLS CUI [1]
C0005910
UMLS CUI [2]
C0005890
negative urine drug and alcohol test
Beskrivning

Urine drug and alcohol test

Datatyp

boolean

Alias
UMLS CUI [1]
C0202274
UMLS CUI [2]
C0868676
willing to follow all study procedures
Beskrivning

Compliance

Datatyp

boolean

Alias
UMLS CUI [1]
C1321605
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
any significant abnormal lab, ecg, medical or physical exam finding during screening
Beskrivning

Laboratory, ECG or physical exam finding

Datatyp

boolean

Alias
UMLS CUI [1]
C0587081
UMLS CUI [2]
C0438154
UMLS CUI [3]
C0031809
allergy to the study drug
Beskrivning

Allergy to study drug

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0304229
excessive alcohol intake
Beskrivning

Substance Use Disorder

Datatyp

boolean

Alias
UMLS CUI [1]
C0038586
positive hiv or hepatitis b or c result
Beskrivning

HIV

Datatyp

boolean

Alias
UMLS CUI [1]
C0019682
UMLS CUI [2]
C0019163
UMLS CUI [3]
C0019196
use of prescription or non-prescription drugs within one week of study start except for birth control
Beskrivning

Pharmacotherapy

Datatyp

boolean

Alias
UMLS CUI [1]
C0013216
blood pressure meds & tylenol
Beskrivning

Antihypertensive agents or tylenol

Datatyp

boolean

Alias
UMLS CUI [1]
C0003364
UMLS CUI [2]
C0699142
pregnant or lactating women
Beskrivning

Gynaecological status

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147

Similar models

Eligibility Hepatitis C, Chronic NCT00439959

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Gender and health status
Item
healthy males & females
boolean
C0079399 (UMLS CUI [1])
C0018759 (UMLS CUI [2])
Age
Item
part 1 ages 18-60
boolean
C0001779 (UMLS CUI [1])
Age specification
Item
part 2 ages 18-50 & 65-80
boolean
C0001779 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
Weight and height
Item
within normal weight range given your height
boolean
C0005910 (UMLS CUI [1])
C0005890 (UMLS CUI [2])
Urine drug and alcohol test
Item
negative urine drug and alcohol test
boolean
C0202274 (UMLS CUI [1])
C0868676 (UMLS CUI [2])
Compliance
Item
willing to follow all study procedures
boolean
C1321605 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Laboratory, ECG or physical exam finding
Item
any significant abnormal lab, ecg, medical or physical exam finding during screening
boolean
C0587081 (UMLS CUI [1])
C0438154 (UMLS CUI [2])
C0031809 (UMLS CUI [3])
Allergy to study drug
Item
allergy to the study drug
boolean
C0020517 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
Substance Use Disorder
Item
excessive alcohol intake
boolean
C0038586 (UMLS CUI [1])
HIV
Item
positive hiv or hepatitis b or c result
boolean
C0019682 (UMLS CUI [1])
C0019163 (UMLS CUI [2])
C0019196 (UMLS CUI [3])
Pharmacotherapy
Item
use of prescription or non-prescription drugs within one week of study start except for birth control
boolean
C0013216 (UMLS CUI [1])
Antihypertensive agents or tylenol
Item
blood pressure meds & tylenol
boolean
C0003364 (UMLS CUI [1])
C0699142 (UMLS CUI [2])
Gynaecological status
Item
pregnant or lactating women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])

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