ID
21172
Beschrijving
Monotherapy Versus Placebo Over 14 or 17 Days in Healthy and Hepatitis C Infected Adults; ODM derived from: https://clinicaltrials.gov/show/NCT00439959
Link
https://clinicaltrials.gov/show/NCT00439959
Trefwoorden
Versies (1)
- 12-04-17 12-04-17 -
Geüploaded op
12 april 2017
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
Model Commentaren :
Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.
Itemgroep Commentaren voor :
Item Commentaren voor :
U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.
Eligibility Hepatitis C, Chronic NCT00439959
Eligibility Hepatitis C, Chronic NCT00439959
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschrijving
Laboratory, ECG or physical exam finding
Datatype
boolean
Alias
- UMLS CUI [1]
- C0587081
- UMLS CUI [2]
- C0438154
- UMLS CUI [3]
- C0031809
Beschrijving
Allergy to study drug
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0304229
Beschrijving
Substance Use Disorder
Datatype
boolean
Alias
- UMLS CUI [1]
- C0038586
Beschrijving
HIV
Datatype
boolean
Alias
- UMLS CUI [1]
- C0019682
- UMLS CUI [2]
- C0019163
- UMLS CUI [3]
- C0019196
Beschrijving
Pharmacotherapy
Datatype
boolean
Alias
- UMLS CUI [1]
- C0013216
Beschrijving
Antihypertensive agents or tylenol
Datatype
boolean
Alias
- UMLS CUI [1]
- C0003364
- UMLS CUI [2]
- C0699142
Beschrijving
Gynaecological status
Datatype
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
Similar models
Eligibility Hepatitis C, Chronic NCT00439959
- StudyEvent: Eligibility
C0018759 (UMLS CUI [2])
C2348235 (UMLS CUI [1,2])
C0005890 (UMLS CUI [2])
C0868676 (UMLS CUI [2])
C0438154 (UMLS CUI [2])
C0031809 (UMLS CUI [3])
C0304229 (UMLS CUI [1,2])
C0019163 (UMLS CUI [2])
C0019196 (UMLS CUI [3])
C0699142 (UMLS CUI [2])
C0006147 (UMLS CUI [2])