Very Rapid and Rapid Virological Response as Predictors of Response of HCV Tretment

Sponsor
Assiut University (Other)
Overall Status
Unknown status
CT.gov ID
NCT03480269
Collaborator
(none)
100
21

Study Details

Study Description

Brief Summary

assessment of very rapid virological response and rapid virological response as predictors of response to sofosbuvir and daclatasvir in treatment of cirrhotic and non-cirrhotic patients with HCV, eligible to treatment.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Chronic hepatitis C infection (CHC) is a global health problem, with an estimated 120 to 130 million chronic hepatitis C virus (HCV) carriers worldwide Therefore, early recognition and effective management of the disease can modify its natural history

    . There is a growing body of evidence that suggests that treatment will help reduce liver inflammation, may reverse liver damage (scarring),slow down disease progression and improve symptoms and quality of life. All of these factors are important reasons to seek HCV medical treatment Identifying host-viral factors that predict the likelihood of SVR prior to initiating therapy would be a very useful clinical tool that could help reduce costs and avoid unnecessary exposure to therapy with significant side effects Little is known about predictors of failure to achieve SVR with DAAs. Although numerous clinical parameters predicted poor response to pegylated IFN treatment , none of them have been shown to be associated with virological relapse after DAA based therapy

    Treatment response terms:

    The ultra rapid virological response (uRVR) is a new endpoint that we defined as an undetectable serum HCV RNA at the end of 1st week of therapy.

    The very rapid virologic response( vRVR )defined as undetectable serum HCV RNA level at week 2.

    The rapid virological response (RVR) defined as undetectable serum HCV RNA after 4 weeks of treatment sustained virological response (SVR), which is defined by the undetectable serum HCV RNA 12-24 weeks after the end of treatment Relapser was defined as undetectable viral load at the end of DAA treatment but subsequent detectable viral load at 12 weeks after treatment end.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    100 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Prospective
    Official Title:
    Very Rapid and Rapid Virological Response as Predictors of Response to Sofosbuvir / Daclatasvir Treatment of HCV Related Liver Disease
    Anticipated Study Start Date :
    Aug 1, 2018
    Anticipated Primary Completion Date :
    Dec 31, 2019
    Anticipated Study Completion Date :
    Apr 30, 2020

    Outcome Measures

    Primary Outcome Measures

    1. Rapid virological response (undetected HCV RNA after 4 weeks from the begin of antiviral treatment) [April 2018 to April 2019]

      To assess rapid virological response as a predictor of response to sofosbuvir and daclatasvir in treatment of cirrhotic and non-cirrhotic patients with HCV. It measure the relation between rapid virological response and achievment of sustained virological response (Undetected HCV RNA 12-24 weeks after the end of treatment )

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Anti HCV positive patients either chronic HCV or liver cirrhosis.

    • Detectable HCV RNA by quantitative PCR prior to treatment.

    • Naïve patients (not received any HCV treatment regimen before)

    Exclusion Criteria:
    • Patients with hepatocellular carcinoma( HCC)

    • Patients with combined HBV and HCV

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Assiut University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Sara Mohammed Mahrous Sayed, Doctor, Assiut University
    ClinicalTrials.gov Identifier:
    NCT03480269
    Other Study ID Numbers:
    • HCV tretment
    First Posted:
    Mar 29, 2018
    Last Update Posted:
    Jul 6, 2018
    Last Verified:
    Mar 1, 2018
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No

    Study Results

    No Results Posted as of Jul 6, 2018