ID
29711
Description
A Study Evaluating 24-Week and 48-Week Telaprevir-Based Regimen in Treatment Naïve Subjects With Genotype 1 Chronic Hepatitis C Who Achieve an Extended Rapid Viral Response; ODM derived from: https://clinicaltrials.gov/show/NCT00758043
Link
https://clinicaltrials.gov/show/NCT00758043
Keywords
Versions (1)
- 4/15/18 4/15/18 -
Copyright Holder
See clinicaltrials.gov
Uploaded on
April 15, 2018
DOI
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License
Creative Commons BY 4.0
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Eligibility Hepatitis C NCT00758043
Eligibility Hepatitis C NCT00758043
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Medical contraindication Pegasys | Medical contraindication Copegus
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1301624
- UMLS CUI [1,2]
- C1176430
- UMLS CUI [2,1]
- C1301624
- UMLS CUI [2,2]
- C1170183
Description
Hepatic decompensation | Subject Cirrhotic
Data type
boolean
Alias
- UMLS CUI [1]
- C1394798
- UMLS CUI [2,1]
- C0681850
- UMLS CUI [2,2]
- C0439686
Description
Organ Transplantation
Data type
boolean
Alias
- UMLS CUI [1]
- C0029216
Description
Medical condition Impact Patient safety
Data type
boolean
Alias
- UMLS CUI [1,1]
- C3843040
- UMLS CUI [1,2]
- C4049986
- UMLS CUI [1,3]
- C1113679
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Eligibility Hepatitis C NCT00758043
- StudyEvent: Eligibility
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C0013216 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
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C0022885 (UMLS CUI [2,1])
C1879533 (UMLS CUI [2,2])
C0031809 (UMLS CUI [3,1])
C1879533 (UMLS CUI [3,2])
C0600109 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2])
C1176430 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C1170183 (UMLS CUI [2,2])
C0681850 (UMLS CUI [2,1])
C0439686 (UMLS CUI [2,2])
C4049986 (UMLS CUI [1,2])
C1113679 (UMLS CUI [1,3])