ID

33822

Descripción

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

Palabras clave

  1. 2/1/19 2/1/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

2 de enero de 2019

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Hepatitis C, Chronic NCT01508156

Eligibility Hepatitis C, Chronic NCT01508156

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
all participants
Descripción

Study Subject All

Tipo de datos

boolean

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

General health good

Tipo de datos

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.
Descripción

Barrier Contraception Double

Tipo de datos

boolean

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

Hepatitis C virus Study Subject

Tipo de datos

boolean

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

Chronic Hepatitis C genotype

Tipo de datos

boolean

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

Exclusion Criteria

Alias
UMLS CUI
C0680251
all participants
Descripción

Study Subject All

Tipo de datos

boolean

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

Pregnancy | Breast Feeding

Tipo de datos

boolean

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

Hepatitis C virus Study Subject

Tipo de datos

boolean

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

Prior Therapy Hepatitis C virus

Tipo de datos

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).
Descripción

HBV coinfection | HIV coinfection

Tipo de datos

boolean

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

Similar models

Eligibility Hepatitis C, Chronic NCT01508156

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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