NCT06530186View on ClinicalTrials.gov

Evaluation of a Postcoital Sponge on Self-Reported Vaginal Health Parameters

NANot yet recruitingINTERVENTIONAL
Enrollment

1,000

Participants

Timeline

Start Date

August 1, 2024

Primary Completion Date

December 31, 2024

Study Completion Date

January 31, 2025

Conditions
Vaginal InfectionVaginal DischargeVaginosisSexual Dysfunction
Interventions
DEVICE

LiviWell Postcoital Vaginal Insert

subjects will use Livi within minutes of completion of sex, and will remove study device in under an hour.

Trial Locations (1)

07046

Garden State Urology, Mountain Lakes

Sponsors
All Listed Sponsors
lead

Atlantic Health System

OTHER