CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 48 enrolled
Drug / intervention
high volume gel +2 moreother
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/NCT01334827
NCT01334827N/ACompleted
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Rational Development of Combination Microbicide Therapies: A Formative Study to Explore the Sensory Perceptions of Vaginal Product Users (Project MIST)

The Miriam Hospital·interventional·Posted Apr 13, 2011·Updated Oct 15, 2025

In Brief

A clinical study evaluating high volume gel, low volume gel, and 1 other intervention for Microbicide Delivery System Acceptability. Completed, enrolled 48 participants across 1 site.

Detailed Summary

The purpose of the study is to compare, contrast, and characterize the range of user perceptions and potential acceptability of three (3) topical vaginal microbicide dosage forms.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMicrobicide Delivery System Acceptability
CountriesUnited States
CollaboratorsImQuest Pharmaceuticals, Inc., National Institute of Allergy and Infectious Diseases (NIAID)

Timeline

N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedApr 13, 2011
Enrollment StartApr 1, 2011
Primary CompletionJun 1, 2012
TodayJul 2, 2026
Enrollment to primary: 1.2 yearsPosted 15.2 years ago

Interventions

high volume gelother

4 mL HEC

low volume gelother

2 mL HEC

vaginal filmother

1" x 2" intravaginal quick-dissolving film