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Completed

NCT Number: NCT05674682

Seroincidence Study Among Men Who Have Sex With Men and Transgender Women - The ImPrEP Seroincidence Study

PrEP (pre-exposure prophylaxis) is an effective prevention strategy in which HIV-negative individuals take antiretroviral drugs (tenofovir disoproxil fumarate and emtricitabine - TDF/FTC) to reduce HIV acquisition. Clinical studies have shown that the TDF/FTC combination protects MSM and transgender women against HIV infection. According to the PROUD study, PrEP can decrease the risk of HIV infection among MSM by 86% (90% CI 64-96). The international community recognizes that PrEP can be an additional tool in the framework of a combination prevention package for those most at risk of contracting HIV. Data on HIV incidence among MSM and trans women are largely unknown. In Brazil, Mexico and Peru, data on the incidence of HIV among MSM and trans women are very scarce, limited to small cross-sectional studies.Current methods used to determine HIV-1 incidence have many limitations. These methods include mathematical modeling, retrospective calculations of AIDS case reports, age-based prevalence determinations, and prevalence determinations with multiple rounds of longitudinal surveys to estimate HIV incidence, which require numerous assumptions and inputs and can pose additional challenges in the era of expansion of antiretroviral therapy (ART) and increased survival of HIV-1 infected individuals. On the other hand, prospective longitudinal cohort studies of high-risk individuals can be used to estimate incidence; however, they are often labor-intensive, complex, very expensive, difficult to implement in most countries, and have recruitment biases. Laboratory methods can be unbiased and do not require complicated assumptions and case-by-case weighting. The cross-sectional use of Recent HIV Infection Tests (TRIs) based on biomarkers offers, in principle, accessible, reliable and low risk of bias options for estimating incidence.

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Key information

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • MSM and transgender women
  • aged 18 years or older
  • willingness and ability to sign an informed consent form.

Exclusion criteria

  • Individuals currently using PrEP, PEP or receiving antiretroviral therapy;
  • Individuals unable to understand the study or who do not agree to sign the consent form;
  • Individuals who are participating in a clinical trial of antiretroviral medication or any investigational product to prevent the acquisition of HIV infection (for example, monoclonal antibodies such as PEP or PrEP)

Treatment and study plan

HIV testing

Procedure

venipuncture or digital puncture for HIV testing

Primary outcomes

  1. Identification of recent infections in a given high-risk population (MSM and TGW), including those in defined geographic areas for evaluate epidemics, calibrate models, design and evaluate interventions.

    Time frame: 2 years

    Blood collected for viral load from those with confirmed HIV infection will be used to distinguish recent HIV-1 infections of long-term infections

Sponsors and collaborators

Lead sponsor

Evandro Chagas National Institute of Infectious Disease

Other

Collaborators

  • Beatriz Grinzstejn, MD, PhD
  • Brenda Hoagland, MD, PhD
  • Carlos Cáceres, MD, MPH, PhD
  • Celia Landmann Szwarcwald, PhD
  • Claudia García-Morales, PhD
  • Giovanni Ravasi, MD, MScPH
  • Hamid Vega-Ramírez, MD, MSc
  • Helleen Vermandere
  • Juan Vicente Guanira, MD, PhD
  • Kelika A. Konda, PhD
  • Marcos Benedetti, MA
  • Maria Cristina Pimenta, MD, PhD
  • Marília Santini Oliveira
  • Nilo Martínez Fernandes, PhD
  • René Leyva-Flores, PhD
  • Ronaldo Ismério Moreira, PhD
  • Sandro Nazer Coutinho
  • Santiago Ávila-Ríos, PhD
  • Sylvia Lopes Maia Teixeira, PhD
  • Sérgio Bautista-Arredondo, MD, PhD
  • Thiago Torres, PhD
  • Valdiléa Veloso dos Santos, Ph.D.

Registry information

Official study title

Seroincidence Study Among Men Who Have Sex With Men and Transgender Women - The ImPrEP Seroincidence Study. A Sub-study of Implementation of HIV Pre-exposure Prophylaxis (PrEP) for Men Who Have Sex With Men and Transgender People: A Demonstration Project in the Context of Combined Prevention in Brazil, Mexico and Peru - the ImPrEP Study

Acronym: Seroincidence

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Jan 6, 2023
Registry last updated
Jan 6, 2023

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.

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