Estimating the Incidence of HIV Infection Among Men Who Have Sex With Men in Peru and Ecuador

National Institute of Allergy and Infectious Diseases (NIAID)2,608 enrolled

Overview

The purpose of this observational study is to estimate the number of new HIV infections and the number and variability of antiretroviral-resistant HIV strains among men who have sex with men (MSM). Participants will be recruited from four sites in Peru and one site in Ecuador.

The governments of Peru and Ecuador signed an agreement with the Global Fund to Fight AIDS, Tuberculosis, and Malaria to help guarantee comprehensive quality of care to people living with HIV, including access to antiretrovirals (ARVs). Current methods of surveillance are inadequate in estimating the true burden of disease. Broad access to ARVs in countries without regular drug resistance testing can also cause rapid development of ARV resistance. By establishing a more sophisticated surveillance system able to capture HIV incidence, prevalence, patterns of HIV resistance, and genetic variability of viral strains, Peru and Ecuador will be better equipped to monitor the HIV epidemic, develop personalized prevention and control measures, and track patterns of HIV resistance among infected patients. This study will estimate the incidence of HIV, syphilis, and herpes simplex virus 2 (HSV-2) among MSM in Peru and Ecuador, as well as examine the number and variability of ARV-resistant HIV strains. This study will last about 2 weeks. Medical history, a physical exam, an HIV rapid test, and HIV pre- and post-test counseling will occur at study entry. Those who test HIV positive will be asked to return to the test site in about 2 weeks to receive confirmatory test results. Patients confirmed to be infected with HIV will be referred to HIV treatment clinics in their area. At study entry, participants will also undergo a syphilis test. Those who test positive for syphilis will receive same-day treatment at the clinic and be asked to return during Week 1 and 2 to complete treatment for sexually transmitted diseases (STDs) according to local guidelines. STD treatment will not be provided by the study. Those who test negative to both the HIV rapid test and the syphilis test at screening will not participate in any more study visits. Patients who consent to having samples stored for further investigations will also have their samples tested for HSV-2 infection following completion of the study.

Study Type

OBSERVATIONAL

Enrollment

2,608

Conditions

HIV Infections Syphilis Sexually Transmitted Diseases

Eligibility

Sex: MALEMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * HIV uninfected or unaware of HIV infection status * Male at birth * Report having anal intercourse, either insertive or receptive, with another man 6 months prior to study entry * Living in one of the participating study cities at time of study entry * Self-report at least one of the following behaviors: * No condom use during the last receptive or insertive anal intercourse * Receptive or insertive anal intercourse with more than five sex partners 6 months prior to study entry * Exchange of money, gifts, drugs, or shelter for sex 6 months prior to study entry * STD symptoms 6 months prior to study entry * Inconsistent condom use with an HIV infected sex partner 6 months prior to study entry Exclusion Criteria: * HIV infected * Unwilling to participate in HIV screening * Any psychiatric or mental condition that may interfere with the study

Locations (6)

Fundación Ecuatoriana Equidad CIPRA CRS

Guayaquil-Guayas, Ecuador

IMPACTA - Miraflores CIPRA CRS

Lima, Peru

IMPACTA - Lince CIPRA CRS

Lima, Peru

IMPACTA - San Miguel CIPRA Project 3B CRS

Lima, Peru

Data from ClinicalTrials.gov

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