Model Towards Elimination of Hepatitis C Infection in Egypt: Feasibility and Effectiveness in 73 Villages - Trial NCT04177043
Access comprehensive clinical trial information for NCT04177043 through Pure Global AI's free database. This Phase 4 trial is sponsored by Egyptian Liver Hospital and is currently Completed. The study focuses on Hepatitis C, Chronic. Target enrollment is 221855 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.
Study Focus
HCV antibody and hepatitis B surface antigen (HBsAg) rapid diagnostic tests
Interventional
diagnostic test
Sponsor & Location
Egyptian Liver Hospital
Timeline & Enrollment
Phase 4
Jun 01, 2015
Dec 01, 2018
Primary Outcome
incidince of HCV in population
Summary
Background: The global response to the HCV infection epidemic has been transformed by the
 availability of low-cost curative short course direct acting antiviral (DAA) therapy. Egypt
 has one of the highest burdens of HCV infection worldwide, and a large treatment programme,
 but reaching rural communities represents a major challenge. We report the feasibility and
 effectiveness of a comprehensive community-based HCV prevention, testing and treatment model
 in 73 villages across Egypt, with the goal to eliminate infection from all adult villagers.
 
 Methods: An HCV educate, test and treat programme was implemented in 73 villages across 7
 governorates in Egypt between 06/2015 and 06/2018. The programme model comprised community
 mobilization facilitated by a network of village promoters to support the education, test and
 treat campaign as well as fund raising in the local community; a comprehensive testing,
 linkage to care and treatment of all eligible villagers aged 12 to 80 years using HCV
 antibody and HBsAg rapid diagnostic tests (RDTs), HCV RNA confirmation of positive cases,
 staging of liver disease using transient elastography (FibroScan), treatment with 12 or 24
 weeks of a direct acting antiviral (DAA) regimen according to national standard of HCV care,
 and an assessment of cure at 12 weeks after completion of treatment (SVR12); and an education
 campaign to raise awareness and disseminate messages about safer practices to reduce
 transmission through public events, promotional materials and house-to-house visits. Key
 outcomes assessed in each village were: uptake of serological HCV and HBV testing, linkage to
 assessment and HCV viral load confirmation, uptake of treatment, and SVR12.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT04177043
Non-Device Trial

