ID
33821
Description
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
Lien
https://clinicaltrials.gov/show/NCT01344889
Mots-clés
Versions (1)
- 02/01/2019 02/01/2019 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
2 janvier 2019
DOI
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Licence
Creative Commons BY 4.0
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Eligibility Hepatitis C, Chronic NCT01344889
Eligibility Hepatitis C, Chronic NCT01344889
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Kidney Failure, Chronic
Type de données
boolean
Alias
- UMLS CUI [1]
- C0022661
Description
Transplantation Organ Major
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0040732
- UMLS CUI [1,2]
- C0178784
- UMLS CUI [1,3]
- C0205164
Description
telbivudine
Type de données
boolean
Alias
- UMLS CUI [1]
- C1453933
Description
Pregnancy | Breast Feeding
Type de données
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
Description
Partner Male Pregnant female
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0682323
- UMLS CUI [1,2]
- C0086582
- UMLS CUI [1,3]
- C0033011
Similar models
Eligibility Hepatitis C, Chronic NCT01344889
- StudyEvent: Eligibility
C0205177 (UMLS CUI [1,2])
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])