ID

34325

Beskrivning

Safety and Efficacy Study of Peginterferon Lambda-1a vs. Peginterferon Alfa-2a, Plus Ribavirin in Subjects With Genotype 1 Hepatitis C; ODM derived from: https://clinicaltrials.gov/show/NCT01754974

Länk

https://clinicaltrials.gov/show/NCT01754974

Nyckelord

  1. 2019-01-16 2019-01-16 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

16 januari 2019

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Hepatitis C Virus (HCV) NCT01754974

Eligibility Hepatitis C Virus (HCV) NCT01754974

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
chronic hepatitis c, genotype 1
Beskrivning

ID.1

Datatyp

boolean

hcv rna ≥100,000 iu/ml at screening
Beskrivning

ID.2

Datatyp

boolean

liver biopsy documenting no cirrhosis (within prior 3 years). where approved for staging of liver disease, non-invasive imaging may be used to assess the extent of liver disease
Beskrivning

ID.3

Datatyp

boolean

naïve to prior anti-hcv therapy
Beskrivning

ID.4

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
infected with hcv other than genotype 1
Beskrivning

ID.5

Datatyp

boolean

positive hepatitis b surface antigen (hbsag), or human immunodeficiency virus (hiv)-1/hiv-2 antibody at screening
Beskrivning

ID.6

Datatyp

boolean

evidence of liver disease other than hcv
Beskrivning

ID.7

Datatyp

boolean

active substance abuse
Beskrivning

ID.8

Datatyp

boolean

use of hematologic growth factors within 90 days prior to study randomization
Beskrivning

ID.9

Datatyp

boolean

evidence of history of cirrhosis based on radiologic criteria or biopsy results and clinical criteria
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Hepatitis C Virus (HCV) NCT01754974

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
chronic hepatitis c, genotype 1
boolean
ID.2
Item
hcv rna ≥100,000 iu/ml at screening
boolean
ID.3
Item
liver biopsy documenting no cirrhosis (within prior 3 years). where approved for staging of liver disease, non-invasive imaging may be used to assess the extent of liver disease
boolean
ID.4
Item
naïve to prior anti-hcv therapy
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
infected with hcv other than genotype 1
boolean
ID.6
Item
positive hepatitis b surface antigen (hbsag), or human immunodeficiency virus (hiv)-1/hiv-2 antibody at screening
boolean
ID.7
Item
evidence of liver disease other than hcv
boolean
ID.8
Item
active substance abuse
boolean
ID.9
Item
use of hematologic growth factors within 90 days prior to study randomization
boolean
ID.10
Item
evidence of history of cirrhosis based on radiologic criteria or biopsy results and clinical criteria
boolean

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