Efficacy Study of the Vaginal Gel Carraguard to Prevent HIV Transmission
This study has been completed.
Sponsor:
Population Council
Collaborators:
United States Agency for International Development (USAID)
Bill and Melinda Gates Foundation
Information provided by (Responsible Party):
Population Council
ClinicalTrials.gov Identifier:
NCT00213083
First received: September 13, 2005
Last updated: May 14, 2012
Last verified: May 2012
| Tracking Information | |||||
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| First Received Date ICMJE | September 13, 2005 | ||||
| Last Updated Date | May 14, 2012 | ||||
| Start Date ICMJE | April 2004 | ||||
| Primary Completion Date | April 2007 (final data collection date for primary outcome measure) | ||||
| Current Primary Outcome Measures ICMJE |
Time to HIV seroconversion during trial participation (evaluated quarterly) | ||||
| Original Primary Outcome Measures ICMJE |
Time to HIV seroconversion during trial participation (evaluated quarterly). | ||||
| Change History | Complete list of historical versions of study NCT00213083 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE |
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| Original Secondary Outcome Measures ICMJE |
Determine long term safety based on genital ulcer disease (evaluated through pelvic exam at all visits), and STI infection. Chlamydia, gonorrhoeae, trichomoniasis and syphilis tests are conducted at months 3, 6, 12, 18 and 24 and as clinically indicated. | ||||
| Current Other Outcome Measures ICMJE | Not Provided | ||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||
| Descriptive Information | |||||
| Brief Title ICMJE | Efficacy Study of the Vaginal Gel Carraguard to Prevent HIV Transmission | ||||
| Official Title ICMJE | Phase 3 Study of the Efficacy and Safety of the Microbicide Carraguard® in Preventing HIV Seroconversion in Women | ||||
| Brief Summary | The purposes of this study are to determine whether Carraguard® Gel can prevent the transmission of HIV when used during vaginal intercourse, and to confirm that the gel is safe for vaginal use. |
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| Detailed Description | This study is designed to show if Carraguard® can protect women against HIV if it is used before sex, and is safe for long-term use. |
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| Study Type ICMJE | Interventional | ||||
| Study Phase | Phase 3 | ||||
| Study Design ICMJE | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Double-Blind Primary Purpose: Prevention |
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| Condition ICMJE |
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| Intervention ICMJE | Drug: Carraguard (PC-515) | ||||
| Study Arm (s) | Not Provided | ||||
| Publications * |
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status ICMJE | Completed | ||||
| Enrollment ICMJE | 6203 | ||||
| Completion Date | April 2007 | ||||
| Primary Completion Date | April 2007 (final data collection date for primary outcome measure) | ||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Female | ||||
| Ages | 16 Years to 40 Years | ||||
| Accepts Healthy Volunteers | Yes | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | South Africa | ||||
| Administrative Information | |||||
| NCT Number ICMJE | NCT00213083 | ||||
| Other Study ID Numbers ICMJE | Population Council #322 | ||||
| Has Data Monitoring Committee | Not Provided | ||||
| Responsible Party | Population Council | ||||
| Study Sponsor ICMJE | Population Council | ||||
| Collaborators ICMJE |
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| Investigators ICMJE |
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| Information Provided By | Population Council | ||||
| Verification Date | May 2012 | ||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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