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Clinical Trials/NCT00514111
NCT00514111
Completed
Not Applicable

Factors Associated to Success of Hepatitis C Therapy

UPECLIN HC FM Botucatu Unesp1 site in 1 country100 target enrollmentStarted: August 2007Last updated:

Overview

Phase
Not Applicable
Status
Completed
Sponsor
UPECLIN HC FM Botucatu Unesp
Enrollment
100
Locations
1

Overview

Brief Summary

The aim of this study is to evaluate the sustained virologic response (RVS) in HVC patients treated with pegylated-interferon or conventional-interferon and ribavirin, and to investigate the associated factors with RVS, by means of retrospective analysis.

Detailed Description

Chronic hepatitis C virus(HVC) is a major public-health problem since it presents a long phase of clinical latency which makes its early diagnosis difficult and results in the development of a large number of cases to complications such as cirrhosis, hepatic insufficiency and hepatocarcinoma. In Brazil, it is estimated three million estimated cases to 52 thousand reports. The aim of this study is to evaluate the sustained virologic response (RVS) in HVC patients treated with pegylated-interferon or conventional-interferon and ribavirin, and to investigate the associated factors with RVS, by means of retrospective analysis.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • HVC patients that received specific treatment with pegylated-interferon or conventional-interferon, and ribavirin

Exclusion Criteria

  • No HVC infection or treatment

Arms & Interventions

HVC Patients

HVC patients attended in SAE e HD.

Intervention: pegylated-interferon, conventional-interferon, ribavirin (Drug)

Investigators

Sponsor
UPECLIN HC FM Botucatu Unesp
Sponsor Class
Other

Study Sites (1)

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