ID

33822

Description

Study of Hepatitis C Virus (HCV) Nonstructural Protein 5a (NS5A) Inhibitor IDX719 in Healthy and HCV-Infected Participants (MK-1894-001); ODM derived from: https://clinicaltrials.gov/show/NCT01508156

Link

https://clinicaltrials.gov/show/NCT01508156

Keywords

  1. 1/2/19 1/2/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

January 2, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Hepatitis C, Chronic NCT01508156

Eligibility Hepatitis C, Chronic NCT01508156

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
all participants
Description

Study Subject All

Data type

boolean

Alias
UMLS CUI [1,1]
C0681850
UMLS CUI [1,2]
C0444868
is in good general health.
Description

General health good

Data type

boolean

Alias
UMLS CUI [1]
C1277245
agrees to use double-barrier method of birth control for at least 90 days after the last dose of study drugs.
Description

Barrier Contraception Double

Data type

boolean

Alias
UMLS CUI [1,1]
C0004764
UMLS CUI [1,2]
C0205173
hcv participants
Description

Hepatitis C virus Study Subject

Data type

boolean

Alias
UMLS CUI [1,1]
C0220847
UMLS CUI [1,2]
C0681850
has documented gt1, gt2, or gt3 chronic hcv infection.
Description

Chronic Hepatitis C genotype

Data type

boolean

Alias
UMLS CUI [1,1]
C0524910
UMLS CUI [1,2]
C1148363
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
all participants
Description

Study Subject All

Data type

boolean

Alias
UMLS CUI [1,1]
C0681850
UMLS CUI [1,2]
C0444868
is pregnant or breastfeeding.
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
hcv participants
Description

Hepatitis C virus Study Subject

Data type

boolean

Alias
UMLS CUI [1,1]
C0220847
UMLS CUI [1,2]
C0681850
has received prior hcv treatment.
Description

Prior Therapy Hepatitis C virus

Data type

boolean

Alias
UMLS CUI [1,1]
C1514463
UMLS CUI [1,2]
C0220847
is co-infected with hepatitis b virus (hbv) and/or human immunodeficiency virus (hiv).
Description

HBV coinfection | HIV coinfection

Data type

boolean

Alias
UMLS CUI [1]
C2242656
UMLS CUI [2]
C4062778

Similar models

Eligibility Hepatitis C, Chronic NCT01508156

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Study Subject All
Item
all participants
boolean
C0681850 (UMLS CUI [1,1])
C0444868 (UMLS CUI [1,2])
General health good
Item
is in good general health.
boolean
C1277245 (UMLS CUI [1])
Barrier Contraception Double
Item
agrees to use double-barrier method of birth control for at least 90 days after the last dose of study drugs.
boolean
C0004764 (UMLS CUI [1,1])
C0205173 (UMLS CUI [1,2])
Hepatitis C virus Study Subject
Item
hcv participants
boolean
C0220847 (UMLS CUI [1,1])
C0681850 (UMLS CUI [1,2])
Chronic Hepatitis C genotype
Item
has documented gt1, gt2, or gt3 chronic hcv infection.
boolean
C0524910 (UMLS CUI [1,1])
C1148363 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Study Subject All
Item
all participants
boolean
C0681850 (UMLS CUI [1,1])
C0444868 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
is pregnant or breastfeeding.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Hepatitis C virus Study Subject
Item
hcv participants
boolean
C0220847 (UMLS CUI [1,1])
C0681850 (UMLS CUI [1,2])
Prior Therapy Hepatitis C virus
Item
has received prior hcv treatment.
boolean
C1514463 (UMLS CUI [1,1])
C0220847 (UMLS CUI [1,2])
HBV coinfection | HIV coinfection
Item
is co-infected with hepatitis b virus (hbv) and/or human immunodeficiency virus (hiv).
boolean
C2242656 (UMLS CUI [1])
C4062778 (UMLS CUI [2])

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