search
Back to results

A Study of Nonoxynol-9 (N-9) and HIV Infection

Primary Purpose

HIV Infections

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Nonoxynol-9
Sponsored by
National Institute of Allergy and Infectious Diseases (NIAID)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for HIV Infections focused on measuring Nonoxynol

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria Volunteers may be eligible if they: Are HIV-negative. Are sexually active and expect to have vaginal intercourse at least twice a week during the study. Are willing to keep a diary of their sexual behavior and N-9 use. Are willing to have regular clinic visits including pelvic exams. Are at least 18 years old. Are female. Exclusion Criteria Volunteers will not be eligible if they: Have had a child or an abortion in the past 42 days. Are allergic to latex or N-9. Have genital sores. Have syphilis, chlamydia, gonorrhea, or trichomoniasis. Are enrolled in another study for a product like N-9. Expect to use another vaginal product other than N-9 during the study. Are pregnant.

Sites / Locations

  • Julia Welch

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 2, 1999
Last Updated
October 27, 2021
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
search

1. Study Identification

Unique Protocol Identification Number
NCT00000926
Brief Title
A Study of Nonoxynol-9 (N-9) and HIV Infection
Official Title
Phase III Nonoxynol-9 and HIV Infection
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
February 2001 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to see if nonoxynol-9 (N-9) gel used in the vagina can prevent the spread of HIV. Most of the people with HIV in the world today live in southern Africa. Because this population is not likely to use condoms, an HIV-prevention method that women can control is needed. N-9 used in the vagina may help prevent the spread of HIV and other sexually transmitted diseases.
Detailed Description
Intravaginal application of N-9 may help protect women from HIV and other STD infection. Low rates of condom use in sub-Saharan African populations, which constitute the majority of HIV infections, dictate the need for prophylactic methods women can control. This trial will be conducted in Zimbabwe and Malawi. The Phase III trial is preceded by a 2-week safety and acceptability pilot study to determine the extent of genital irritation caused by N-9 and the placebo. Following the pilot study and prior to screening for enrollment in the Phase III trial, potential volunteers will participate in a 2-month behavioral counseling program that will encourage the use of condoms. Only participants who decide they cannot or will not be consistent condom users are enrolled in the main study. Study participants are given N-9 gel or placebo to use each time they have vaginal sexual intercourse for 18 to 36 months. Participants have a follow-up evaluation once a month; a pelvic exam and blood tests are performed every third month.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Nonoxynol

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Masking
Double
Enrollment
4400 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Nonoxynol-9

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria Volunteers may be eligible if they: Are HIV-negative. Are sexually active and expect to have vaginal intercourse at least twice a week during the study. Are willing to keep a diary of their sexual behavior and N-9 use. Are willing to have regular clinic visits including pelvic exams. Are at least 18 years old. Are female. Exclusion Criteria Volunteers will not be eligible if they: Have had a child or an abortion in the past 42 days. Are allergic to latex or N-9. Have genital sores. Have syphilis, chlamydia, gonorrhea, or trichomoniasis. Are enrolled in another study for a product like N-9. Expect to use another vaginal product other than N-9 during the study. Are pregnant.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Taha E.Taha
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Nancy Padian
Official's Role
Study Chair
Facility Information:
Facility Name
Julia Welch
City
Research Triangle Park
State/Province
North Carolina
ZIP/Postal Code
27709
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
16773032
Citation
Kumwenda N, Hoffman I, Chirenje M, Kelly C, Coletti A, Ristow A, Martinson F, Brown J, Chilongozi D, Richardson B, Rosenberg Z, Padian N, Taha T. HIV incidence among women of reproductive age in Malawi and Zimbabwe. Sex Transm Dis. 2006 Nov;33(11):646-51. doi: 10.1097/01.olq.0000223283.27142.9f.
Results Reference
result

Learn more about this trial

A Study of Nonoxynol-9 (N-9) and HIV Infection

We'll reach out to this number within 24 hrs