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Hepatitis C Reinfection After Successful Directly Acting Antiviral Treatment: A Belgian Interventional Multicenter Study
The primary aim of this study is to calculate the incidence of HCV reinfection after successful DAA treatment among people who have recently injected drugs. The secondary aim is to identify factors associated with reinfection in this population. Individuals with active injecting drug abuse with a chronic HCV infection who have achieved end of treatment response (ETR; defined as non-detectable HCV RNA at end of treatment) to any interferon-free DAA combination will be included in this multicenter interventional study.
This protocol is an adapted version of the protocol 'Hepatitis C reinfection after successful directly acting antiviral treatment: A North-Atlantic multicenter interventional study'. The investigators will plan this study so that the data are similar to this protocol and results can be compared within this alliance of hepatologists with special interest in care for substance users. Study schedule: Data collection will be performed according to the study schedule shown in Table 1. Following assessment for SVR12, participants will be followed for 2 years at 6 months' intervals at the discretion of each study site.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Free Clinic Antwerp
Antwerp, Belgium
ZNA Stuivenberg
Antwerp, Belgium
CHU Saint-Pierre
Brussels, Belgium
Ziekenhuis Oost-Limburg
Genk, Belgium
AZ Maria-Middelares
Ghent, Belgium
CAD Limburg
Hasselt, Belgium
Jessa Ziekenhuis
Hasselt, Belgium
CHC Saint-Josephe, Liège
Liège, Belgium
Sint-Trudo Ziekenhuis
Sint-Truiden, Belgium
AZ Vesalius
Tongeren, Belgium
Start Date
July 1, 2019
Primary Completion Date
February 28, 2022
Completion Date
February 28, 2022
Last Updated
August 26, 2021
100
ESTIMATED participants
Blood sampling
OTHER
questionaires
OTHER
Lead Sponsor
Hasselt University
Collaborators
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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