MedPath

Prospective and Retrospective Multicenter Cohort Study of Patients With Chronic Hepatitis C Treated by Peginterferon Alfa-2b Plus Ribaviri

Phase 4
Conditions
Chronic Hepatitis C
Registration Number
JPRN-UMIN000003976
Lead Sponsor
Department of Gastroenterology The University of Tokyo Hospital
Brief Summary

The rate of SVR was 55%.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up continuing
Sex
All
Target Recruitment
150
Inclusion Criteria

Not provided

Exclusion Criteria

Any contraindication to peginterferon alfa-2b + ribavirin therapy

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sustained virological response 24 weeks after the end of treatment
Secondary Outcome Measures
NameTimeMethod
Safety
© Copyright 2025. All Rights Reserved by MedPath