A Formative Study to Explore the Sensory Perceptions of Vaginal Product Users

NACompletedINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

April 30, 2011

Primary Completion Date

June 30, 2012

Study Completion Date

June 30, 2012

Conditions
Microbicide Delivery System Acceptability
Interventions
OTHER

high volume gel

4 mL HEC

OTHER

low volume gel

2 mL HEC

OTHER

vaginal film

"1 x 2 intravaginal quick-dissolving film"

Trial Locations (1)

02906

Miriam Hospital, Providence

Sponsors
All Listed Sponsors
collaborator

ImQuest Pharmaceuticals, Inc.

INDUSTRY

collaborator

National Institute of Allergy and Infectious Diseases (NIAID)

NIH

lead

The Miriam Hospital

OTHER