CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 84 enrolled
Drug / intervention
No intervention (not applicable)other
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01231763
NCT01231763N/ACompleted

Film Acceptability Characterization and Evaluation

University of Pittsburgh·observational·Posted Nov 1, 2010·Updated Feb 9, 2011

In Brief

An observational study evaluating No intervention (not applicable) for HIV Infections and Anti-Infective Agents. Completed, enrolled 84 participants across 2 sites.

Detailed 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.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedNov 1, 2010
Enrollment StartNov 1, 2010
Primary CompletionFeb 1, 2011
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 15.7 years ago

Interventions

No intervention (not applicable)other

No intervention (not applicable)