Clinical Trial

Seville Cohort of People at Substantial Risk for HIV Infection on Pre-exposure Prophylaxis

Study acronym: SeVIHPrEP
Enrolling by Invitation
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Summary
Pre-exposure prophylaxis (PrEP) based on tenofovir represents a considerably new preventive intervention that has shown to significantly decrease the number of HIV infections while it enables early diagnosis of HIV and other sexually transmitted diseases (STI). In Southern Spain, the target population to receive PrEP are men who have sex with men (MSM) with a history of STI and who pursue high-risk sexual practices regarding the acquisition of HIV, including an elevate number of sex partners, no or inconsistent condom use and the use of specific recreational drugs in the context of sexual activity ("chemsex"). Despite the benefits of PrEP use, it must be taken into consideration that risk compensations that may facilitate the acquisition of other STI may occur, including a higher implementation of risk practices and an increase in the number of partners, which is made easy as various social networks designed for this purpose are available nowadays. In order to better understand the benefit/drawback ratio, accurate data of a population using PrEP under real-life conditions, with densely scheduled follow-up and well-characterized (socio-)demographic parameters, sexual behaviour and STI are warranted.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2022-08-05.
Trial Details
NCT Number NCT05492565
Lead Sponsor Hospitales Universitarios Virgen del Rocío
Collaborators: Instituto de Biomedicina de Sevilla
Conditions HIV Infection Primary, Hepatitis, Viral, Human, Sexually Transmitted Infections, Excluding HIV and Hepatitis
Enrollment 500 participants
Start Date 2020-01-01
Primary Completion 2029-12-31 (estimated)
Study Completion 2030-12-31 (estimated)
Updated on ClinicalTrials.gov 2023-09-22