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NCT01231763 · ClinicalTrials.gov registry record
Acceptability Study of Vaginal Films for HIV Prevention
A clinical trial, sponsored by University of Pittsburgh.
- Completed
- Registry status
- 84
- Enrollment target
NCT01231763: Completed study, sponsored by University of Pittsburgh.
NCT01231763 is a clinical trial that has completed, run by University of Pittsburgh. The registered enrollment target is 84 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01231763 has completed, sponsored by University of Pittsburgh.
- COMPLETED
- Registry status
- 84 participants
- Enrollment target
Study Summary
This study is being done to find out what women would want in a film vaginal product for human immunodeficiency virus (HIV) prevention, especially what it should look like and how to apply it. The investigators hypothesize that women will prefer a smooth, clear, and rectangular quick-dissolve vaginal film for HIV prevention over a textured, opaque, square quick-dissolve vaginal film.
Primary Outcome
Preferred texture, shape, size, and appearance of a vaginal film product via focus group discussion and questionnaires
Interventions
- OTHER No intervention (not applicable)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 84 participants |
| Start Date | 2010-11 |
| Est. Completion | 2011-02 |
What the finished NCT01231763 record still lists
NCT01231763 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 84 participants, a relatively small participant target.
The record links to 0 conditions, and to 1 intervention - of which No intervention (not applicable) is the first listed.
NCT01231763 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01231763 about?
NCT01231763 is a clinical study titled "Acceptability Study of Vaginal Films for HIV Prevention". This study is being done to find out what women would want in a film vaginal product for human immunodeficiency virus (HIV) prevention, especially what it should look like and how to apply it. The investigators hypothesize that women will prefer a smooth, clear, and rectangular quick-dissolve vagin...
What is the current status of trial NCT01231763?
This trial is currently completed. The enrollment target is 84 participants. The study started on 2010-11. Estimated completion is 2011-02.
What interventions are being tested in trial NCT01231763?
The interventions under investigation include: No intervention (not applicable) (OTHER).
Who is sponsoring clinical trial NCT01231763?
This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.
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