Last updated on February 2018

Prevention of HIV in " le-de-France"


Brief description of study

Interventional HIV prevention strategy based on pre-exposure prophylaxis (PrEP) with Truvada for people in the le-de-France area (or Paris region) who don't have HIV but who are at high risk of becoming infected with HIV (men who have sex with men (MSM), transgender men and women, heterosexual men and women, sex workers, migrants) in combination with overall prevention services (communautary-based or educational counselling; addiction, social and psychological care; condoms and lubricating gel; clean injection equipment; sexually transmitted diseases (STD) screening and treatment; hepatitis A virus (HAV), hepatitis B virus (HBV) and hepatitis C virus (HCV) vaccinations and post-exposure treatment of HIV infection as soon as possible after diagnosis using an antiretroviral combination recommended by the French Guidelines on HIV treatment).

The individual benefit being already demonstrated in clinical trials, the aim is to demonstrate the public health impact of the interventional HIV prevention strategy by reducing the risk of getting HIV-1 infection of at least 15% of new diagnosis of HIV infections among MSM/transgender in the Ile-de-France area after a 3-year period.

Detailed Study Description

Assuming the PrEP efficacy of 80% and that 85% of included participants being MSM - the objective is to evidence a decrease of at least 15% of new diagnosis of HIV infections among MSM in Ile-de-France area. This objective is in the framework of a commitment of large cities against AIDS with the political support of the City of Paris for the "Paris sans SIDA" program and the commitment of the le-de-France area.

Secondary Objectives:

  • Prevalence of HIV infection at the screening visit (undiagnosed epidemic)
  • Incidence of HIV infection according to back-calculation approach, and by key subgroups

Operational Objectives:

  • Evaluate the origin of the recruitment according to the risk groups and the outreach actions
  • Assess linkage to care for PrEP, retention in the study, reasons for consent withdrawal and satisfaction of the participants according to the screening site, the type of PrEP supply, the costs of global care, the key subgroups, the type of counselling, the time from STD testing to initiation of PrEP treatment in study sites
  • Impact of a less intense counselling than the one provided in the ANRS IPERGAY trial, on adherence and efficacy of PrEP by comparing the incidence observed in MSM enrolled in the current study to that evidenced in the ANRS IPERGAY trial, with a method similar to that used in the Partner demonstration project in Kenya and Uganda.
  • Impact of the communautary-based and educational counselling

Clinical Objectives:

  • Estimation, in individuals seeking for PrEP and thus getting tested for HIV infection, the prevalence of HIV infection in different key subgroups, which is a surrogate marker of the undiagnosed (or "hidden") epidemic
  • Evaluate who will become HIV-infected during the course of the study while on PrEP, the proportion of patients on combined antiretroviral treatment and the proposition of patients with a suppressed HIV viral load 12 months after HIV infection
  • Evaluate the participants' need for post-exposure prophylaxis during the course of the study
  • Adherence to PrEP (questionnaire and dried blood spots)
  • Assessment of the PrEP dosing schedule used by MSM participants (daily or intermittent) throughout the course of the study
  • Assessment of PrEP tolerability and safety
  • Comprehensive study of incident HIV infections in those on PrEP (incidence, emergence of drug-associated resistance mutations, adherence to PrEP at the closest visit before HIV seroconversion and at previous visits)

Participants Behavior:

  • Acceptability of PrEP (including those who will decline participation in the study) and during the course of the study, and retention in the study.
  • Impact of PrEP, within a comprehensive prevention offer, on sexual behavior of the participants throughout follow-up
  • Factors associated with the integration of PrEP in the daily routine of participants:
    • Qualitative study to explore the motivations, difficulties, behavior and expectations of the participants, their knowledge and communication on their use of PrEP
    • Reasons related to the choice of the prevention strategy used in terms of dosing schedule (continuous or on demand in MSM) and type of counselling and participation to focus groups.

Care Providers Behavior: Evaluation of knowledge, beliefs, perception and practice of the physicians, nurse and peer counselors involved in delivery of PrEP in the study

Social epidemiology: Evaluation of social and/or territorial inequalities and disparities

Cost-effectiveness of the comprehensive prevention strategy

Clinical Study Identifier: NCT03113123

Find a site near you

Start Over

H pital Foch

Suresnes, France
2.11miles
  Connect »

CHI Poissy Saint Germain en Laye

Saint Germain en Laye, France
3.94miles
  Connect »

H pital Ambroise-Par

Boulogne, France
4.13miles
  Connect »

H pital Louis Mourier

Colombes, France
4.13miles
  Connect »

H pital Andr Mignot

Versailles, France
5.97miles
  Connect »

H pital Antoine B cl re

Clamart, France
6.8miles
  Connect »

H pital Cochin

Paris, France
7.58miles
  Connect »

H pital H tel Dieu

Paris, France
8.17miles
  Connect »

H pital Tenon

Paris, France
8.17miles
  Connect »

H pital de Bic tre

Le Kremlin Bicêtre, France
9.6miles
  Connect »

Recruitment Status: Open


Brief Description Eligibility Contact Research Team


Receive Emails About New Clinical Trials!

Sign up for our FREE service to receive email notifications when clinical trials are posted in the medical category of interest to you.