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Effect of Combination Therapy with Ledipasvir and Sofosbuvir (Hepasbuvir Plus) for Treatment of Patients with Hepatitis C Infectio

Phase 2
Conditions
Chronic hepatitis C infection.
Chronic viral hepatitis C
Registration Number
IRCT2016050717413N15
Lead Sponsor
Baqiyatallah Research Center for Gastroenterology and Liver Diseases, Baqiyatallah University of Med
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
30
Inclusion Criteria

Inclusion Criteria: Iranian patients with genotype-1 hepatitis C virus infection; with minimum age of 18 year old; with or without previous history of treatment (Peg-Interferon, Ribavirin, Protease inhibitors including: Telaprevir and Boceprevir); Compensated or Decompensated Cirrhosis;

Exclusion Criteria

Co-infection with HIV infection; Patients with thalassemia; Patients with hemophilia; Patients with history of chronic hemodialysis; patients with history of liver transplantation

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Hepatitis C Viral load. Timepoint: Before starting therapy, 4 weeks after starting therapy, end of therapy, 4 weeks after end of therapy, 12 weeks after end of therapy. Method of measurement: Quantitative viral load in laboratory.
Secondary Outcome Measures
NameTimeMethod
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