Acceptability Study of Vaginal Films for HIV Prevention

Completed

Conditions studied: HIV Infections, Anti-Infective Agents

In brief

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.

Key facts

Study ID

NCT01231763

Run by

University of Pittsburgh

People needed

84

Starts

2010-11-01

Expected to finish

2011-02-01

Last updated by the study team

2011-02-09

Who can join

Age: 18 and older, up to 30. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Female 18-30 years old at time of enrollment
• Able to provide written informed consent

You may not qualify if…

• Not sexually active, defined as no vaginal sex at any time in the past year
• Pregnant by self-report

Where it is running

• Magee-Womens Hospital of UPMC — Pittsburgh, Pennsylvania, United States
• Magee-Womens Research Institute — Pittsburgh, Pennsylvania, United States

Full record on ClinicalTrials.gov

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