ID

33822

Beschrijving

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

Trefwoorden

  1. 02-01-19 02-01-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

2 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Hepatitis C, Chronic NCT01508156

Eligibility Hepatitis C, Chronic NCT01508156

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
all participants
Beschrijving

Study Subject All

Datatype

boolean

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

General health good

Datatype

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.
Beschrijving

Barrier Contraception Double

Datatype

boolean

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

Hepatitis C virus Study Subject

Datatype

boolean

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

Chronic Hepatitis C genotype

Datatype

boolean

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

Exclusion Criteria

Alias
UMLS CUI
C0680251
all participants
Beschrijving

Study Subject All

Datatype

boolean

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

Pregnancy | Breast Feeding

Datatype

boolean

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

Hepatitis C virus Study Subject

Datatype

boolean

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

Prior Therapy Hepatitis C virus

Datatype

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).
Beschrijving

HBV coinfection | HIV coinfection

Datatype

boolean

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

Similar models

Eligibility Hepatitis C, Chronic NCT01508156

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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