ID
21172
Description
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
Keywords
Versions (1)
- 4/12/17 4/12/17 -
Uploaded on
April 12, 2017
DOI
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License
Creative Commons BY 4.0
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Eligibility Hepatitis C, Chronic NCT00439959
Eligibility Hepatitis C, Chronic NCT00439959
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Laboratory, ECG or physical exam finding
Data type
boolean
Alias
- UMLS CUI [1]
- C0587081
- UMLS CUI [2]
- C0438154
- UMLS CUI [3]
- C0031809
Description
Allergy to study drug
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0304229
Description
Substance Use Disorder
Data type
boolean
Alias
- UMLS CUI [1]
- C0038586
Description
HIV
Data type
boolean
Alias
- UMLS CUI [1]
- C0019682
- UMLS CUI [2]
- C0019163
- UMLS CUI [3]
- C0019196
Description
Pharmacotherapy
Data type
boolean
Alias
- UMLS CUI [1]
- C0013216
Description
Antihypertensive agents or tylenol
Data type
boolean
Alias
- UMLS CUI [1]
- C0003364
- UMLS CUI [2]
- C0699142
Description
Gynaecological status
Data type
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])