Clinical Trials in France / NCT05361603
Recruiting
Observational
Acceptability of Simultaneous Screening for Viral Hepatitis B, C and HIV Among Drug Users in Non-conventional Structures
NCT05361603 · tracked via the Priya Life Science France tracker
Condition(s) studied
Hepatitis CTransmission, Intravenous Drug AbuserAddiction, AlcoholAddiction OpiateHepatitis C Virus Infection, Response to Therapy of
Study summary
The principle is to propose dedicated monthly screening days bringing together the health personnel involved (hepatologist, addictologist, nurse in charge of the program, addictology nurse and social worker) and to propose appropriate management for each situation assessed.
Eligibility
Inclusion Criteria:
* Adult 18 and over
* Patient frequenting an unconventional structure "outside the walls" or referred by a professional in the care sector
* Patient who agreed to participate to the research
Exclusion Criteria:
* Patient doesn't agree to participate to the research
Primary outcome measure(s)
- Number of RTDs performed compared to the number proposed — up to 10 years
Evaluate the acceptability of simultaneous screening for viral hepatitis B, C and HIV among drug users in non-conventional structures using a dual method by RTDs and FibroScan® - Number of FibroScan® performed compared to the number proposed — up to 10 years
Evaluate the acceptability of simultaneous screening for viral hepatitis B, C and HIV among drug users in non-conventional structures using a dual method by RTDs and FibroScan®
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Chu Limoges | Limoges | Haute Vienne | Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05361603 on ClinicalTrials.gov ↗ ← All trials in France