ID

34330

Descripción

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

Palabras clave

  1. 16/1/19 16/1/19 -
Titular de derechos de autor

see on clinicaltrials.gov

Subido en

16 de enero de 2019

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Hepatitis C, Chronic NCT01884402

Eligibility Hepatitis C, Chronic NCT01884402

Inclusion Criteria
Descripción

Inclusion Criteria

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

ID.1

Tipo de datos

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.
Descripción

ID.2

Tipo de datos

boolean

patients genotype 1 and 4.
Descripción

ID.3

Tipo de datos

boolean

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

ID.4

Tipo de datos

boolean

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

ID.5

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

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

ID.6

Tipo de datos

boolean

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

ID.7

Tipo de datos

boolean

patients with co-infection with hepatitis b.
Descripción

ID.8

Tipo de datos

boolean

patients with other liver diseases.
Descripción

ID.9

Tipo de datos

boolean

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

ID.10

Tipo de datos

boolean

Similar models

Eligibility Hepatitis C, Chronic NCT01884402

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