Evaluation of a Non-Implanted Electrical Stimulation Device for Overactive Bladder (OAB)
Recruiting now · Not applicable
Conditions studied: Overactive Bladder (OAB)
In brief
A study to evaluate the safety and effectiveness of FemPulse System
Key facts
- Study ID
- NCT07195656
- Run by
- FemPulse Corporation
- People needed
- 151
- Starts
- 2025-09-30
- Expected to finish
- 2027-12-31
- Last updated by the study team
- 2026-07-13
Who can join
Age: 21 and older. Sex: female. Healthy volunteers: not accepted.
Where it is running
- Southern Urogynecology — West Columbia, South Carolina, United States (enrolling)
- Sanford Health — Sioux Falls, South Dakota, United States (enrolling)
- Cedars Sinai — Beverly Hills, California, United States (enrolling)
- Stanford — Palo Alto, California, United States (enrolling)
- USCD — San Diego, California, United States (enrolling)
- Holy Cross Medical Group - Women's Center — Fort Lauderdale, Florida, United States (enrolling)
- Comprehensive Urologic — Barrington, Illinois, United States (enrolling)
- UCLA — Los Angeles, California, United States (enrolling)
- Chesapeake Urology — Owings Mills, Maryland, United States (enrolling)
- UC Irvine — Orange, California, United States (enrolling)
- Adult & Pediatric Urology — Omaha, Nebraska, United States (enrolling)
- Atrium Health — Charlotte, North Carolina, United States (enrolling)
- INOVA — Falls Church, Virginia, United States
- University of Louisville — Louisville, Kentucky, United States
- Minnesota Urology — Woodbury, Minnesota, United States
Full record on ClinicalTrials.gov
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