ID

34191

Description

Herpes Simplex Type 1 Suppression in Hepatitis C; ODM derived from: https://clinicaltrials.gov/show/NCT01580995

Link

https://clinicaltrials.gov/show/NCT01580995

Keywords

  1. 1/15/19 1/15/19 -
  2. 5/14/19 5/14/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 15, 2019

DOI

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License

Creative Commons BY-NC 3.0

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Eligibility Chronic Hepatitis C Infection NCT01580995

Eligibility Chronic Hepatitis C Infection NCT01580995

Inclusion Criteria
Description

Inclusion Criteria

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

ID.1

Data type

boolean

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

ID.2

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

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

ID.3

Data type

boolean

hiv or chronic hepatitis b infection,
Description

ID.4

Data type

boolean

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

ID.5

Data type

boolean

creatinine clearance <50 ml/min.,
Description

ID.6

Data type

boolean

female subject who is pregnant or nursing,
Description

ID.7

Data type

boolean

gastrointestinal disorder which might result in malabsorption of valacyclovir,
Description

ID.8

Data type

boolean

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

ID.9

Data type

boolean

allergy to valacyclovir or related drug.
Description

ID.10

Data type

boolean

Similar models

Eligibility Chronic Hepatitis C Infection NCT01580995

Name
Type
Description | Question | Decode (Coded Value)
Data type
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

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