ID

34330

Beschrijving

Observational,Prospective Study to Develop and Validate a Prognostic Tool to Optimize Therapy in Patients With HCV G1/4; ODM derived from: https://clinicaltrials.gov/show/NCT01884402

Link

https://clinicaltrials.gov/show/NCT01884402

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 C, Chronic NCT01884402

Eligibility Hepatitis C, Chronic NCT01884402

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with > 18 years old.
Beschrijving

ID.1

Datatype

boolean

patients diagnosed with chronic hepatitis c in the presence of hcv rna in plasma that meet criteria for initiating antiviral therapy in routine clinical practice conditions.
Beschrijving

ID.2

Datatype

boolean

patients genotype 1 and 4.
Beschrijving

ID.3

Datatype

boolean

patients with the results of all the factors evaluable at the time of inclusion.
Beschrijving

ID.4

Datatype

boolean

patients who have accepted their participation in the study through informed consent.
Beschrijving

ID.5

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients previously treated with interferon (ifn) and ribavirin (rbv).
Beschrijving

ID.6

Datatype

boolean

patients with genotype 2, 3, 5 and 6.
Beschrijving

ID.7

Datatype

boolean

patients with co-infection with hepatitis b.
Beschrijving

ID.8

Datatype

boolean

patients with other liver diseases.
Beschrijving

ID.9

Datatype

boolean

patients with any contraindications to the drugs used in the treatment of hepatitis
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Hepatitis C, Chronic NCT01884402

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patients with > 18 years old.
boolean
ID.2
Item
patients diagnosed with chronic hepatitis c in the presence of hcv rna in plasma that meet criteria for initiating antiviral therapy in routine clinical practice conditions.
boolean
ID.3
Item
patients genotype 1 and 4.
boolean
ID.4
Item
patients with the results of all the factors evaluable at the time of inclusion.
boolean
ID.5
Item
patients who have accepted their participation in the study through informed consent.
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
patients previously treated with interferon (ifn) and ribavirin (rbv).
boolean
ID.7
Item
patients with genotype 2, 3, 5 and 6.
boolean
ID.8
Item
patients with co-infection with hepatitis b.
boolean
ID.9
Item
patients with other liver diseases.
boolean
ID.10
Item
patients with any contraindications to the drugs used in the treatment of hepatitis
boolean

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