An Imaging Trial of the Distribution of Topical Gel Formulations in the Human Vagina
Status unconfirmed · Phase 1
Conditions studied: HIV Infections
In brief
This study is designed to assess the distribution and spread of four different vehicle formulations in the vagina. In-vivo data will be obtained regarding each vehicle formulation at various time points after insertion of the gel into the vagina.
Key facts
- Study ID
- NCT00214747
- Run by
- Biosyn
- People needed
- 6
- Starts
- 2005-03-01
- Expected to finish
- 2005-11-01
- Last updated by the study team
- 2005-10-25
Who can join
Age: 18 and older, up to 45. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- 18 to 45 year old women
- non-pregnant
- healthy
You may not qualify if…
- abnormal finding on pelvic exam
- pregnant or breastfeeding
- allergy to intravaginal products
- history of claustrophobia
Where it is running
- Rreproductive Research Unit, U of Penn Medical Center — Philadelphia, Pennsylvania, United States
Full record on ClinicalTrials.gov
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