ID
16442
Beschrijving
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
Trefwoorden
Versies (1)
- 16-07-16 16-07-16 -
Geüploaded op
16 juli 2016
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Hepatitis C NCT00328549
Eligibility Hepatitis C NCT00328549
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschrijving
hiv-infected patients
Datatype
boolean
Alias
- UMLS CUI [1]
- C0019699
Beschrijving
history of any primary hematologic disease
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0018939
- UMLS CUI [1,2]
- C0277554
Beschrijving
attributable anemia
Datatype
boolean
Alias
- UMLS CUI [1]
- C0162316
- UMLS CUI [2]
- C0497165
Beschrijving
hemolysis or gastrointestinal bleeding
Datatype
boolean
Alias
- UMLS CUI [1]
- C0019054
- UMLS CUI [2]
- C0017181
Beschrijving
other hepatic disease
Datatype
boolean
Alias
- UMLS CUI [1]
- C0023895
Beschrijving
hcv
Datatype
boolean
Alias
- UMLS CUI [1]
- C0220847
Beschrijving
active substance use disorder
Datatype
boolean
Alias
- UMLS CUI [1]
- C0038586
Beschrijving
pregnant or breast feeding
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0549206
- UMLS CUI [1,2]
- C0006147
Beschrijving
birth control measures
Datatype
boolean
Alias
- UMLS CUI [1]
- C0700589
Beschrijving
epoetin alfa
Datatype
boolean
Alias
- UMLS CUI [1]
- C0357126
Beschrijving
recent transfusions
Datatype
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])