Eligibility Chronic Hepatitis C Infection NCT01580995

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
chronic hepatitis c infection with a detectable hcv rna in the serum on two occasions, 6 months apart
Descripción

ID.1

Tipo de datos

boolean

focus hsv-2 igg negative and focus hsv-1 igg positive, using manufacturer's cut-offs
Descripción

ID.2

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
antiherpes or immunomodulatory therapy during the past 30 days,
Descripción

ID.3

Tipo de datos

boolean

hiv or chronic hepatitis b infection,
Descripción

ID.4

Tipo de datos

boolean

decompensated liver disease (ascites, hepatic encephalopathy, coagulopathy, jaundice/icterus),
Descripción

ID.5

Tipo de datos

boolean

creatinine clearance <50 ml/min.,
Descripción

ID.6

Tipo de datos

boolean

female subject who is pregnant or nursing,
Descripción

ID.7

Tipo de datos

boolean

gastrointestinal disorder which might result in malabsorption of valacyclovir,
Descripción

ID.8

Tipo de datos

boolean

history of erythema multiforme major, thrombotic thrombocytopenia purpura or hemolytic uremic syndrome,
Descripción

ID.9

Tipo de datos

boolean

allergy to valacyclovir or related drug.
Descripción

ID.10

Tipo de datos

boolean

Similar models

Eligibility Chronic Hepatitis C Infection NCT01580995

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
chronic hepatitis c infection with a detectable hcv rna in the serum on two occasions, 6 months apart
boolean
ID.2
Item
focus hsv-2 igg negative and focus hsv-1 igg positive, using manufacturer's cut-offs
boolean
Item Group
C0680251 (UMLS CUI)
ID.3
Item
antiherpes or immunomodulatory therapy during the past 30 days,
boolean
ID.4
Item
hiv or chronic hepatitis b infection,
boolean
ID.5
Item
decompensated liver disease (ascites, hepatic encephalopathy, coagulopathy, jaundice/icterus),
boolean
ID.6
Item
creatinine clearance <50 ml/min.,
boolean
ID.7
Item
female subject who is pregnant or nursing,
boolean
ID.8
Item
gastrointestinal disorder which might result in malabsorption of valacyclovir,
boolean
ID.9
Item
history of erythema multiforme major, thrombotic thrombocytopenia purpura or hemolytic uremic syndrome,
boolean
ID.10
Item
allergy to valacyclovir or related drug.
boolean