ID
16442
Description
A Study to Evaluate the Erythropoietic Response in Hepatitis C Virus (HCV) Patients Receiving Combination Ribavirin (RBV)/Interferon (IFN) Therapy or RBV/PEG IFN (NATURAL HISTORY-HCV); ODM derived from: https://clinicaltrials.gov/show/NCT00328549
Link
https://clinicaltrials.gov/show/NCT00328549
Keywords
Versions (1)
- 7/16/16 7/16/16 -
Uploaded on
July 16, 2016
DOI
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License
Creative Commons BY 4.0
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Eligibility Hepatitis C NCT00328549
Eligibility Hepatitis C NCT00328549
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
hiv-infected patients
Data type
boolean
Alias
- UMLS CUI [1]
- C0019699
Description
history of any primary hematologic disease
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0018939
- UMLS CUI [1,2]
- C0277554
Description
attributable anemia
Data type
boolean
Alias
- UMLS CUI [1]
- C0162316
- UMLS CUI [2]
- C0497165
Description
hemolysis or gastrointestinal bleeding
Data type
boolean
Alias
- UMLS CUI [1]
- C0019054
- UMLS CUI [2]
- C0017181
Description
other hepatic disease
Data type
boolean
Alias
- UMLS CUI [1]
- C0023895
Description
hcv
Data type
boolean
Alias
- UMLS CUI [1]
- C0220847
Description
active substance use disorder
Data type
boolean
Alias
- UMLS CUI [1]
- C0038586
Description
pregnant or breast feeding
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0549206
- UMLS CUI [1,2]
- C0006147
Description
birth control measures
Data type
boolean
Alias
- UMLS CUI [1]
- C0700589
Description
epoetin alfa
Data type
boolean
Alias
- UMLS CUI [1]
- C0357126
Description
recent transfusions
Data type
boolean
Alias
- UMLS CUI [1]
- C0005841
Similar models
Eligibility Hepatitis C NCT00328549
- StudyEvent: Eligibility
C1971490 (UMLS CUI [1,2])
C0205539 (UMLS CUI [2,1])
C0035525 (UMLS CUI [2,2])
C0279030 (UMLS CUI [2,3])
C0277554 (UMLS CUI [1,2])
C0497165 (UMLS CUI [2])
C0017181 (UMLS CUI [2])
C0006147 (UMLS CUI [1,2])