ID

34330

Description

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

Keywords

  1. 1/16/19 1/16/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 16, 2019

DOI

To request one please log in.

License

Creative Commons BY 4.0

Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Eligibility Hepatitis C, Chronic NCT01884402

Eligibility Hepatitis C, Chronic NCT01884402

Inclusion Criteria
Description

Inclusion Criteria

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

ID.1

Data type

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.
Description

ID.2

Data type

boolean

patients genotype 1 and 4.
Description

ID.3

Data type

boolean

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

ID.4

Data type

boolean

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

ID.5

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

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

ID.6

Data type

boolean

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

ID.7

Data type

boolean

patients with co-infection with hepatitis b.
Description

ID.8

Data type

boolean

patients with other liver diseases.
Description

ID.9

Data type

boolean

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

ID.10

Data type

boolean

Similar models

Eligibility Hepatitis C, Chronic NCT01884402

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

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial