HIV Prevention Preparedness Study

National Institute of Allergy and Infectious Diseases (NIAID)

Status: Completed

Conditions: HIV Infections; HIV Seronegativity

Study type: Observational

Funder types: NIH

Identifiers

NCT00048282

HIVNET/HPTN 055

Details and patient eligibility

About

The purpose of this study is to provide researchers with information that will help them prepare for a future study to test the efficacy of two anti-HIV vaginal gels. This study will also estimate how likely people living in certain areas are to become infected with HIV and other infections passed during sex.

Full description

This study is designed to prepare for the implementation of a second study, HPTN 035: A Phase II/III Safety and Effectiveness Study of the Vaginal Microbicides BufferGel and PRO 2000/5 Gel (P) for the Prevention of HIV Infection in Women. HPTN 035 requires an average HIV seroincidence rate of 5-6 percent among enrolled participants. The primary objective of the present study is to estimate the rates of HIV seroincidence among women targeted for inclusion in HPTN 035.

Women will be enrolled in this study for 6 to 12 months. Study visits will take place monthly. At each visit, participants will complete a medical/menstrual history and undergo pregnancy testing. Each quarter, participants will undergo a structured interview about sexual practices and will receive HIV and STD tests, education, and counseling. Participants will also undergo a pelvic exam with wet mount testing for bacterial vaginosis, candidiasis, and trichomoniasis. Colposcopic evaluations will be performed at selected sites. Pap smears will be performed at sites with the capacity and expertise to prepare and interpret the smears and provide appropriate follow-up care to participants with abnormal results.

Sex: Female

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Sexually active (defined as having had vaginal intercourse at least once in the 3 months prior to screening).
• HIV-uninfected at screening.
• Able and willing to provide adequate locator information for study retention purposes.

Exclusion criteria

• History of adverse reaction to latex.
• Non-therapeutic injection drug use in the 12 months prior to screening.
• Vaginal intercourse more than an average of 2 times per day in the 2 weeks prior to screening.
• Plans to travel away from the study site for more than 3 consecutive months in the next 12 months.
• Plans to relocate away from the study site in the next 12 months.
• Pregnancy or plans to become pregnant in the next 12 months.
• Pregnancy within 42 days prior to enrollment.
• Enrollment in any other study of a vaginally-applied product.
• Clinically apparent pelvic exam finding involving deep epithelial disruption.
• Diagnosis with a current STD and/or other reproductive tract infection requiring treatment.
• Conditions that would preclude provision of informed consent, make participation in the study unsafe, complicate interpretation of study outcome data, or otherwise interfere with achieving the study objectives.