ID

34331

Beschrijving

A Study of Pegasys (Peginterferon Alfa 2a) Alone or in Combination With Tenofovir in Patients With Chronic Hepatitis D.; ODM derived from: https://clinicaltrials.gov/show/NCT01088659

Link

https://clinicaltrials.gov/show/NCT01088659

Trefwoorden

  1. 16-01-19 16-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

16 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Hepatitis D, Chronic NCT01088659

Eligibility Hepatitis D, Chronic NCT01088659

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
adult patients, >/=18 years of age
Beschrijving

ID.1

Datatype

boolean

chronic hepatitis d
Beschrijving

ID.2

Datatype

boolean

positive for hbsag >/=6 months, for anti-hdv >/=3 months and for hdv-rna at screening
Beschrijving

ID.3

Datatype

boolean

negative pregnancy test; fertile males and women of childbearing age should use two reliable forms of contraception throughout study
Beschrijving

ID.4

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
antiviral therapy for chronic hepatitis d within the previous 6 months
Beschrijving

ID.5

Datatype

boolean

previous therapy with pegylated interferon alfa
Beschrijving

ID.6

Datatype

boolean

treatment with conventional interferon alfa for >12 months
Beschrijving

ID.7

Datatype

boolean

hepatitis a or c, or hiv infection
Beschrijving

ID.8

Datatype

boolean

decompensated liver disease (childs b-c)
Beschrijving

ID.9

Datatype

boolean

history or evidence of medical condition associated with chronic liver disease
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Hepatitis D, Chronic NCT01088659

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
adult patients, >/=18 years of age
boolean
ID.2
Item
chronic hepatitis d
boolean
ID.3
Item
positive for hbsag >/=6 months, for anti-hdv >/=3 months and for hdv-rna at screening
boolean
ID.4
Item
negative pregnancy test; fertile males and women of childbearing age should use two reliable forms of contraception throughout study
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
antiviral therapy for chronic hepatitis d within the previous 6 months
boolean
ID.6
Item
previous therapy with pegylated interferon alfa
boolean
ID.7
Item
treatment with conventional interferon alfa for >12 months
boolean
ID.8
Item
hepatitis a or c, or hiv infection
boolean
ID.9
Item
decompensated liver disease (childs b-c)
boolean
ID.10
Item
history or evidence of medical condition associated with chronic liver disease
boolean

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