NCT06347380View on ClinicalTrials.gov

Usability Study of the FemPulse System

NARecruitingINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

September 11, 2024

Primary Completion Date

December 30, 2025

Study Completion Date

December 30, 2025

Conditions
Overactive Bladder
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 (2)

33334

RECRUITING

Holy Cross Women's Hospital, Fort Lauderdale

98133

RECRUITING

Univ. of Washington, Seattle

Sponsors
All Listed Sponsors
lead

FemPulse Corporation

INDUSTRY