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NCT00028132 · ClinicalTrials.gov registry record · Phase 1
Safety and Acceptability of the Anti-Microbe Vaginal Gel, PMPA Gel
A Phase 1 study of HIV Infections, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).
- Completed
- Registry status
- Phase 1
- Development phase
- 120
- Enrollment target
- 5
- Study locations
NCT00028132: Completed Phase 1 study of HIV Infections, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).
NCT00028132 is a Phase 1 study of HIV Infections that has completed, run by National Institute of Allergy and Infectious Diseases (NIAID). The registered enrollment target is 120 participants, below the 446-participant average among 542 other HIV Infections trials with a reported enrollment target (73% lower). The trial reports 5 study locations across 3 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00028132, a Phase 1 study of HIV Infections, has completed, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 120 participants
- Enrollment target
- 5
- Study locations
Study Summary
The purpose of this study is to evaluate the PMPA gel, which kills microbes, in HIV-infected and HIV-uninfected women. The majority of new HIV infections occur through heterosexual contact. A product that stops or slows the replication of HIV during sexual contact is needed. At present, there are no products that are completely effective. PMPA gel, also known as tenofovir, is an anti-microbe agent that may fight against sexual transmission of HIV and other sexually transmitted diseases (STDs). It is applied to the vagina and gives women the ability to control their disease-prevention activity.
Conditions Studied
Interventions
- DRUG Tenofovir
Study Locations (5)
New York
- Harlem Prevention Ctr. CRS (El-Sadr CTU) - New York
- Bronx- Lebanon Hospital Center Clinical Research Site (BLHC CRS) - The Bronx
Rhode Island
- The Miriam Hosp., Div. of Infectious Disease - Providence
- Women & Infants' Hosp. - Providence
Pennsylvania
- 3535 Market Street CRS - Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 120 participants |
| Est. Completion | 2005-12 |
| Phase | Phase 1 |
What the finished NCT00028132 record still lists
NCT00028132 is an interventional study that assigns participants to a tested intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap, below the 446-participant average among 542 other HIV Infections trials with a reported enrollment target (73% lower).
The record links to 1 condition, with HIV Infections appearing as the primary indexed condition, and to 1 intervention - of which Tenofovir is the first listed.
NCT00028132 lists 5 locations in 3 states (New York, Rhode Island, Pennsylvania).
Frequently Asked Questions
What is clinical trial NCT00028132 about?
NCT00028132 is a clinical study titled "Safety and Acceptability of the Anti-Microbe Vaginal Gel, PMPA Gel". The purpose of this study is to evaluate the PMPA gel, which kills microbes, in HIV-infected and HIV-uninfected women. The majority of new HIV infections occur through heterosexual contact. A product that stops or slows the replication of HIV during sexual contact is needed. At present, there are n...
What is the current status of trial NCT00028132?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 120 participants. Estimated completion is 2005-12.
What conditions does trial NCT00028132 study?
This clinical trial studies the following conditions: HIV Infections.
What interventions are being tested in trial NCT00028132?
The interventions under investigation include: Tenofovir (DRUG).
Who is sponsoring clinical trial NCT00028132?
This trial is sponsored by National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00028132 being conducted?
This trial has 5 study locations across New York, Pennsylvania, Rhode Island. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for HIV Infections
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT00028132's enrollment target sits among peer trials
120 239th of 542 higher than 295 of 542 other HIV Infections trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other HIV Infections trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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