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Evaluation of Pre-Exposure Prophylaxis Against HIV in Alpine Region (PrEP2A)

C

Centre Hospitalier Annecy Genevois

Status

Completed

Conditions

Pre-Exposure Prophylaxis
Drug Combination
HIV Seronegativity

Treatments

Other: Questionnaire

Study type

Observational

Funder types

Other

Identifiers

NCT03995862
2018-A02993-52 (Other Identifier)
18-39-PrEP2A

Details and patient eligibility

About

Despite the implementation of a national strategy to prevent the transmission of the human immunodeficiency virus (HIV) combining prevention campaigns, condom use, early detection of HIV infections and recommendations for treatment as soon as possible, the number of new HIV-infected patients per year in France does not decrease.

New HIV prevention strategies are therefore clearly needed. Since 2009, several studies have shown that tenofovir disoproxil fumarate and emtricitabine (TDF/FTC), an antiretroviral therapy combining two nucleoside reverse transcriptase inhibitors used for the treatment of patients seropositive for HIV, has preventive activity on HIV transmission. These results enabled the TDF/FTC to obtain in France an extension of the marketing authorization in March 2017 for preexposure prophylaxis (PrEP) of HIV transmission among patients at high risk of contamination.

Since the approval, many studies around the world investigate the use of PrEP in routine practice, highlighting its effectiveness in real life. These studies describe the population of patients who benefit from PrEP in order to adapt their multidisciplinary care but also track the transmission of other sexually transmitted infections to prevent their emergence, given the observed decline in condom use. However, these studies are limited to big cities while PrEP is accessible in all territories.

The Rhône-Alpes region is one of the three French regions that has been the most involved in the implementation of PrEP, one year after the FTC/TDF approval in France. Given the geographical position of the investigators, both in province and close to Switzerland, where the FTC/TDF is not authorized for PrEP, and the non-university nature of five of the six involved hospitals, the investigators would like to determine the profile of patients consulting in this region to benefit from PrEP. This analysis will also determine if the population at risk of the "Alpine Arc" region is similar to that observed in the other cohorts in order to adapt patient care.

Enrollment

242 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient having initiated or wishing to initiate PrEP according to the recommendations of the French High Authority of Health in the centers involved in the collection of data
  • Patient informed of the study and having indicated his non opposition for the collection of his health data

Exclusion criteria

  • Wardship patient
  • Patient under curatorship
  • Patient unable to give his non-opposition to the use of his health data

Trial design

242 participants in 1 patient group

Patients in care, at high risk of HIV infection
Description:
Patients in care, at high risk of HIV infection, according to the criteria defined by the French Ministry Of Health for the use of FTC / TDF in PreP (men who have sex with men, transgender, heterosexual women migrants or not, sex workers (sexual intercourse in exchange for money, drugs, housing, food), intravenous drug users) HIV-negative, exposed by their sexual practices to a high risk of HIV infection.
Treatment:
Other: Questionnaire

Trial contacts and locations

6

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Central trial contact

Emilie Piet, MD; Marion Noret

Data sourced from clinicaltrials.gov

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