NCT06885099 - Ease of Use Study of the FemPulse System | Biotech Hunter

Enrollment

Participants

Timeline

Start Date

February 11, 2025

Primary Completion Date

August 31, 2025

Study Completion Date

August 31, 2025

Conditions

Overactive Bladder (OAB)

Interventions

DEVICE

FemPulse System

Subjects to receive the FemPulse System consisting of a non-implanted, vaginal electrical stimulation device (Ring) and other patient accessories.

Trial Locations (1)

RECRUITING

Holy Cross Women's Hospital, Fort Lauderdale