Eligibility Hepatitis C, Chronic NCT01057667

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
adult patients, 18-70 years of age
Beskrivning

ID.1

Datatyp

boolean

hepatitis c, genotype 1 or 4, of over 6 months duration
Beskrivning

ID.2

Datatyp

boolean

treatment-naïve
Beskrivning

ID.3

Datatyp

boolean

negative pregnancy test; female patients of childbearing age and male patients with female partners of childbearing age must use two forms of contraception during treatment and following the last dose of ribavirin in accordance with locally approved label for ribavirin
Beskrivning

ID.4

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or breast feeding females or male partners of pregnant females
Beskrivning

ID.5

Datatyp

boolean

previous interferon or ribavirin based therapy or investigational anti-hcv agent
Beskrivning

ID.6

Datatyp

boolean

systemic antiviral therapy with established or perceived activity against hcv </=3 months prior to first dose of study drug
Beskrivning

ID.7

Datatyp

boolean

hepatitis a or b, or hiv infection
Beskrivning

ID.8

Datatyp

boolean

history or evidence of medical condition associated with chronic liver disease other than hcv
Beskrivning

ID.9

Datatyp

boolean

Similar models

Eligibility Hepatitis C, Chronic NCT01057667

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
adult patients, 18-70 years of age
boolean
ID.2
Item
hepatitis c, genotype 1 or 4, of over 6 months duration
boolean
ID.3
Item
treatment-naïve
boolean
ID.4
Item
negative pregnancy test; female patients of childbearing age and male patients with female partners of childbearing age must use two forms of contraception during treatment and following the last dose of ribavirin in accordance with locally approved label for ribavirin
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
pregnant or breast feeding females or male partners of pregnant females
boolean
ID.6
Item
previous interferon or ribavirin based therapy or investigational anti-hcv agent
boolean
ID.7
Item
systemic antiviral therapy with established or perceived activity against hcv </=3 months prior to first dose of study drug
boolean
ID.8
Item
hepatitis a or b, or hiv infection
boolean
ID.9
Item
history or evidence of medical condition associated with chronic liver disease other than hcv
boolean