Actively Recruiting

Age: 18Years +
All Genders
ID06431945

Early Detection of Hepatitis C in Injection Drug Users

Led by Institute of Health Information and Statistics of the Czech Republic · Updated on 2025-06-29

3000

Participants Needed

18

Research Sites

N/A

Total Duration

On this page

Sponsors

I

Institute of Health Information and Statistics of the Czech Republic

Lead Sponsor

I

Institute for Clinical and Experimental Medicine

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are conducting a national, prospective, multicenter, non-interventional pilot project to screen for Hepatitis C virus (HCV) infection among people who inject drugs (PWID) in the Czech Republic. The main goal is to prepare, implement, and assess a method for early detection of Hepatitis C and to develop new procedures for integrating this screening into social health care systems. This project aims to help prevent further transmission of the virus by improving early diagnosis and care continuity.

CONDITIONS

Brief Title

Early Detection of HCV in Injection Drug Users

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Active injecting drug user or history of injecting drug use at any time in the past
Not Eligible

You will not qualify if you...

  • Not agreeing to participate in the project

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person) for hepatitis C antibody test

Diagnostic Evaluation

Duration - Up to 1 week

Participants with a positive hepatitis C antibody test undergo further testing to confirm infection using hepatitis C RNA and genotype tests.

1 follow-up visit (in-person) for confirmatory RNA and genotype tests

Long-term Monitoring

Duration - Until 31 December 2025

Participants who undergo routine care are observed to monitor the incidence of hepatitis C virus and evaluate early detection methods.

Follow-up visits as needed depending on care and monitoring

Trial Site Locations

Total: 18 locations

1

Brno University Hospital

Brno, Czechia

Actively Recruiting

2

Clinic Podane ruce

Brno, Czechia

Actively Recruiting

3

České Budějovice Hospital

České Budějovice, Czechia

Actively Recruiting

4

Hospital Havířov

Havířov, Czechia

Actively Recruiting

5

Hepatogastroenterology Hradec Kralove

Hradec Králové, Czechia

Actively Recruiting

6

University Hospital Hradec Kralove

Hradec Králové, Czechia

Actively Recruiting

7

Hospital Jihlava

Jihlava, Czechia

Actively Recruiting

8

Regional Hospital Karlovy Vary

Karlovy Vary, Czechia

Actively Recruiting

9

University Hospital Olomouc

Olomouc, Czechia

Actively Recruiting

10

Hospital Opava

Opava, Czechia

Actively Recruiting

11

Hospital Pardubice

Pardubice, Czechia

Actively Recruiting

12

Institute for Clinical and Experimental Medicine

Prague, Czechia

Actively Recruiting

13

Military University Hospital, Prague

Prague, Czechia

Actively Recruiting

14

Remedis Prague

Prague, Czechia

Actively Recruiting

15

Hospital Agel Prostějov

Prostějov, Czechia

Actively Recruiting

16

Hospital Tábor

Tábor, Czechia

Actively Recruiting

17

Masarykova Nemocnice v Usti nad Labem, Krajska Zdravotni a.s.

Ústí nad Labem, Czechia

Actively Recruiting

18

Tomáš Baťa Regional Hospital in Zlín

Zlín, Czechia

Actively Recruiting

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Research Team

N

Nikola Stourac

L

Lucie Mandelova, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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