ID

34329

Beschrijving

Hepatic Safety of Raltegravir Versus Efavirenz as HIV Therapy for Patients With HIV and HCV Coinfection; ODM derived from: https://clinicaltrials.gov/show/NCT01147107

Link

https://clinicaltrials.gov/show/NCT01147107

Trefwoorden

  1. 16-01-19 16-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

16 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Hepatitis C, Chronic NCT01147107

Eligibility Hepatitis C, Chronic NCT01147107

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
hiv infected patients, age >18 years, meet vietnam guideline to begin art (cd4 count < 350 cells/mm3 and/or who stage iii or iv disease)
Beschrijving

ID.1

Datatype

boolean

hepatitis c infection as documented by positive hcv antibodies and a detectable serum hcv rna level
Beschrijving

ID.2

Datatype

boolean

ast and alt ≤ 2 x uln (≤ 80 u/l)
Beschrijving

ID.3

Datatype

boolean

estimated creatinine clearance ≥ 60 ml/min
Beschrijving

ID.4

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
any prior art
Beschrijving

ID.5

Datatype

boolean

positive hepatitis b surface antigen
Beschrijving

ID.6

Datatype

boolean

clinical evidence of de-compensated cirrhosis (ascites, encephalopathy, esophageal bleeding)
Beschrijving

ID.7

Datatype

boolean

requirement for acute therapy for other aids-defining illness within 14 days prior to study entry
Beschrijving

ID.8

Datatype

boolean

currently on rifampicin therapy
Beschrijving

ID.9

Datatype

boolean

in the first trimester of pregnancy, intent to become pregnant, or breast feeding during the study period
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Hepatitis C, Chronic NCT01147107

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
hiv infected patients, age >18 years, meet vietnam guideline to begin art (cd4 count < 350 cells/mm3 and/or who stage iii or iv disease)
boolean
ID.2
Item
hepatitis c infection as documented by positive hcv antibodies and a detectable serum hcv rna level
boolean
ID.3
Item
ast and alt ≤ 2 x uln (≤ 80 u/l)
boolean
ID.4
Item
estimated creatinine clearance ≥ 60 ml/min
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
any prior art
boolean
ID.6
Item
positive hepatitis b surface antigen
boolean
ID.7
Item
clinical evidence of de-compensated cirrhosis (ascites, encephalopathy, esophageal bleeding)
boolean
ID.8
Item
requirement for acute therapy for other aids-defining illness within 14 days prior to study entry
boolean
ID.9
Item
currently on rifampicin therapy
boolean
ID.10
Item
in the first trimester of pregnancy, intent to become pregnant, or breast feeding during the study period
boolean

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