Viewing Study NCT00000927



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Last Modification Date: 2024-10-26 @ 9:02 AM
Study NCT ID: NCT00000927
Status: COMPLETED
Last Update Posted: 2007-01-09
First Post: 1999-11-02

Brief Title: A Study of BufferGel in Women
Sponsor: National Institute of Allergy and Infectious Diseases NIAID
Organization: National Institute of Allergy and Infectious Diseases NIAID

Study Overview

Official Title: Phase I Vaginal Microbicide Study of BufferGel
Status: COMPLETED
Status Verified Date: 1999-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to see if it is safe to use BufferGel in the vaginas of women who do not have HIV and who have a low risk of getting HIV

Many new cases of HIV are the result of heterosexual activity Condom use is currently the only effective way of preventing the spread of HIV and other sexually transmitted diseases STDs However women who have a greater risk of getting HIV are often unable to convince their partner to use a condom Therefore it is important to develop methods that prevent the spread of HIV and that are controlled by the woman such as medicines used in the vagina BufferGel is known to kill the organisms that cause STDs including HIV BufferGel may do this without causing genital irritation and sores as other medicines do More studies are needed to see if this is true
Detailed Description: Heterosexual transmission of HIV presently accounts for the vast majority of new HIV infections worldwide Currently the condom is the only method available that has been shown to be effective against HIV and other sexually transmitted diseases STDs However women who are at the greatest risk for acquiring HIV are often unable to negotiate condom use Therefore it is important that effective female-controlled barrier methods such as topical microbicides be made available to women BufferGel has sufficient buffer capacity to acidify twice its own volume in human semen which inactivates STD pathogens including HIV Unlike most other topical microbicides BufferGel is non-detergent so it should not cause genital irritation and lesions The safety and acceptability of BufferGel still need to be studied more carefully

Participants are divided into two cohorts Cohort IA consists of sexually abstinent women and cohort IB consists of sexually active women Within each US cohort participants are assigned to apply BufferGel either once or twice daily Within each international cohort all participants apply BufferGel twice daily Participants apply BufferGel for 14 days Pelvic examinations are performed at Days 7 and 14

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?: