ID

34327

Descrizione

Study of the Anti-HCV Drug (BMS-790052) Combined With Peginterferon and Ribavirin in Patients Who Failed Prior Treatment; ODM derived from: https://clinicaltrials.gov/show/NCT01170962

collegamento

https://clinicaltrials.gov/show/NCT01170962

Keywords

  1. 16/01/19 16/01/19 -
Titolare del copyright

see on clinicaltrials.gov

Caricato su

16 gennaio 2019

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0

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Eligibility Hepatitis C Virus NCT01170962

Eligibility Hepatitis C Virus NCT01170962

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
subjects chronically infected with hcv genotype 1
Descrizione

ID.1

Tipo di dati

boolean

non-responder to prior therapy with peginterferon alfa and ribavirin
Descrizione

ID.2

Tipo di dati

boolean

hcv rna viral load of ≥ 100,00 iu/ml
Descrizione

ID.3

Tipo di dati

boolean

results of a liver biopsy ≤ 24 months prior to randomization consistent with chronic hcv infection; for compensated cirrhotics can be any time prior to randomization (compensated cirrhotics will be capped at 10% of randomized study population)
Descrizione

ID.4

Tipo di dati

boolean

ultrasound, ct scan or mri results 12 months prior to randomization that do not demonstrate hepatocellular carcinoma
Descrizione

ID.5

Tipo di dati

boolean

body mass index (bmi) of 18 to 35 kg/m2
Descrizione

ID.6

Tipo di dati

boolean

Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
positive for hepatitis b infection (hbsag) or hiv-1/hiv-2 antibody at screening
Descrizione

ID.7

Tipo di dati

boolean

evidence of medical condition associated with chronic liver disease other than hcv
Descrizione

ID.8

Tipo di dati

boolean

evidence of decompensated cirrhosis based on radiologic criteria or biopsy
Descrizione

ID.9

Tipo di dati

boolean

Similar models

Eligibility Hepatitis C Virus NCT01170962

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
subjects chronically infected with hcv genotype 1
boolean
ID.2
Item
non-responder to prior therapy with peginterferon alfa and ribavirin
boolean
ID.3
Item
hcv rna viral load of ≥ 100,00 iu/ml
boolean
ID.4
Item
results of a liver biopsy ≤ 24 months prior to randomization consistent with chronic hcv infection; for compensated cirrhotics can be any time prior to randomization (compensated cirrhotics will be capped at 10% of randomized study population)
boolean
ID.5
Item
ultrasound, ct scan or mri results 12 months prior to randomization that do not demonstrate hepatocellular carcinoma
boolean
ID.6
Item
body mass index (bmi) of 18 to 35 kg/m2
boolean
Item Group
C0680251 (UMLS CUI)
ID.7
Item
positive for hepatitis b infection (hbsag) or hiv-1/hiv-2 antibody at screening
boolean
ID.8
Item
evidence of medical condition associated with chronic liver disease other than hcv
boolean
ID.9
Item
evidence of decompensated cirrhosis based on radiologic criteria or biopsy
boolean

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