Skip to main content
OpenTrials
Recruiting

NCT Number: NCT05361603

Acceptability of Simultaneous Screening for Viral Hepatitis B, C and HIV Among Drug Users in Non-conventional Structures

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.

Recruiting

Interested in participating?

Request Info

Key information

About this study

  • Information on screening, the days are announced by :
  • Mailing to health professionals in the Haute-Vienne Department,
  • Announcement to the different professional orders concerned (doctors, pharmacists, midwives, nurses, etc.),
  • Flyers and posters in health care facilities,
  • Distribution in the AddictLim network newsletter (pharmacists, nurses, social workers members),
  • Various: Liaison team, health delegate of the network, intranet site of the hospital, CCAS, AMPA, day care centers.
  • Conduct of a SCANVIR day in the non-conventional structure " Hors les murs " :

Each patient presenting during the screening day will have an individualized welcome.

Addictological and hepatological data will be collected throughout the process by the various workers on the individual Scanvir form (attached).

  • The patient accepts one or more of the examinations proposed as part of the routine care. After information, he/she does not object to the collection of his/her personal data.
  • One or more TRODs and a FibroScan® are performed by the nurse in charge of the care pathway and/or the facility.
  • Performing, by the biologist or the authorized person, the delocalized PCR in case of positive HCV TROD
  • Consultation with the hepatologist, who gives the results of the TROD and FibroScan® in a closed and dedicated place where the confidentiality of exchanges is guaranteed.
  • A written document with the results of the TROD and FibroScan® and GeneXpert is given to the patient.

Method for routine management of patients according to results :

  • HCV HBV HIV TROD are negative and FibroScan® > 7.1 KPa:

The patient meets directly with the hepatologist to screen for risk factors for chronic liver disease (alcohol, medications ...).

  • The HCV HBV HIV TROD are negative and the FibroScan ® < 7.1 KPa :

The nurse at the facility reviews with the patient the modes of transmission of the viruses and discusses with him/her risk reduction and harm reduction and what to do in case of recent exposure.

  • Positive HCV TROD:

The hepatologist offers to do an immediate and on-site HCV RNA by delocalized PCR (GeneXpert). If the HCV RNA is positive, HCV treatment is started immediately (excluding comorbidity). An appointment is proposed 3 months after treatment to control the cure by delocalized PCR on site (RVS12)

  • HIV or HBV TROD positivity:

The hepatologist proposes to do immediately and on site a complete blood test (HIV serology, HBV serologies (HBsAg, HBcAb, HBsAb) by the nurse present, assesses other risk factors and schedules an appointment for the results and management.

For all situations, a prevention action to reduce the risks of transmission of HCV and HBV will be carried out at the same time.

An anti-viral B vaccination may be offered.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. Number of RTDs performed compared to the number proposed

    Time frame: 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®

  2. Number of FibroScan® performed compared to the number proposed

    Time frame: 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®

Secondary outcomes

  1. Number of days actually completed and the number of participants per session

    Time frame: up to 10 years

    Evaluate the feasibility of simultaneous screening for viral hepatitis B, C and HIV in drug users in non-conventional structures using a dual screening method TROD and FibroScan®

  2. Number and proportion of patients having accepted the immediate consultation with the hepatologist and/or with an addictologist

    Time frame: up to 10 years

    Evaluate the acceptability of risk reduction methods as part of the care pathway.

  3. Number of patients who had social care

    Time frame: up to 10 years

    Evaluate the impact of screening in terms of patient care.

  4. Number of anti-viral B vaccinations offered and carried out

    Time frame: up to 10 years

    Evaluate the impact of screening in terms of patient care.

  5. Number of GeneXperts performed compared to the number proposed

    Time frame: up to 10 years

    Evaluate the impact of screening in terms of patient care.

  6. The number and proportion of HCV or HBV antiviral treatments initiated in patients screened positive and having a therapeutic indication

    Time frame: up to 10 years

    Evaluate the impact of screening in terms of patient care.

  7. Therapeutic compliance with anti-HCV treatments and sustained virological response rate in treated patients,

    Time frame: up to 10 years

    Evaluate the impact of screening in terms of patient care.

  8. The absolute number and proportion of patients treated or not maintained in the care pathway in treated patients

    Time frame: up to 10 years

    Evaluate the impact of screening in terms of patient care.

Study contacts

Contact information is provided by the study sponsor or research team.

Marilyne DEBETTE-GRATIEN, MD

CONTACT

[email protected]

33 5 55 05 87 26

Véronique LOUSTAUD-RATTI, Prof

CONTACT

[email protected]

33 5 55 05 66 84

Sponsors and collaborators

Lead sponsor

University Hospital, Limoges

Other

Registry information

Official study title

Acceptability of Simultaneous Screening for Viral Hepatitis B, C and HIV Among Drug Users in Non-conventional Facilities "Outside the Walls" Using the Dual Screening Method TROD (Rapid Diagnostic Tests) and FibroScan

Acronym: SCANVIR

Important dates

Study start
2017
Primary completion
2022
Study completion
2030
First posted
May 4, 2022
Registry last updated
May 4, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.