ID
33821
Beschrijving
An Observational Study on The Prediction of Adverse Events in Patients With Chronic Hepatitis C Receiving a Long-Acting Interferon Plus Ribavirin (GUARD-C); ODM derived from: https://clinicaltrials.gov/show/NCT01344889
Link
https://clinicaltrials.gov/show/NCT01344889
Trefwoorden
Versies (1)
- 02-01-19 02-01-19 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
2 januari 2019
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Hepatitis C, Chronic NCT01344889
Eligibility Hepatitis C, Chronic NCT01344889
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschrijving
Kidney Failure, Chronic
Datatype
boolean
Alias
- UMLS CUI [1]
- C0022661
Beschrijving
Transplantation Organ Major
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0040732
- UMLS CUI [1,2]
- C0178784
- UMLS CUI [1,3]
- C0205164
Beschrijving
telbivudine
Datatype
boolean
Alias
- UMLS CUI [1]
- C1453933
Beschrijving
Pregnancy | Breast Feeding
Datatype
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
Beschrijving
Partner Male Pregnant female
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0682323
- UMLS CUI [1,2]
- C0086582
- UMLS CUI [1,3]
- C0033011
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Eligibility Hepatitis C, Chronic NCT01344889
- StudyEvent: Eligibility
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C0443252 (UMLS CUI [1,3])
C0035525 (UMLS CUI [2])
C0332197 (UMLS CUI [1,2])
C3652465 (UMLS CUI [1,3])
C3652465 (UMLS CUI [2,1])
C0205177 (UMLS CUI [2,2])
C0443252 (UMLS CUI [2,3])
C1301624 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C0035525 (UMLS CUI [3,3])
C0178784 (UMLS CUI [1,2])
C0205164 (UMLS CUI [1,3])
C0006147 (UMLS CUI [2])
C0086582 (UMLS CUI [1,2])
C0033011 (UMLS CUI [1,3])