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Safety and Efficacy of Different Antiviral Regimens for Hepatitis C Virus Relapse

Hepatitis C Clinical Trial

Official title:
Safety and Efficacy of Directly Acting Antiviral Agents in Genotype 4 Hepatitis C Virus Relapse Among Egyptian Patients

Clinical Trial Summary

The primary goal of hepatitis C virus (HCV) Direct Acting Antivirals (DAAs) is to achieve undetectable HCV RNA in the blood. A response that should be maintained for at least 12 weeks from completion of therapy. This is called sustained virological response (SVR) which corresponds to cure of HCV infection as risk of later relapse is very small. SVR is important to achieve improvement in liver necroinflammation and fibrosis and to decrease complications of cirrhosis. Failing to achieve SVR after treatment requires another regimen for these experienced patients. Real-world data are always needed to evaluate and improve our practices. Here investigators aim to assess tolerability and efficacy of different regimens used for management of genotype 4 HCV relapse.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04662138
Study type Observational
Source Alexandria University
Contact Ahmed Kamal
Phone 01279734654
Email Ahmed.Kamal@alexmed.edu.eg
Status Recruiting
Phase
Start date August 24, 2020
Completion date May 28, 2022
View Details
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