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Evaluation of a Non-Implanted Electrical Stimulation Device for Overactive Bladder (OAB)
Sponsor: FemPulse Corporation
Summary
A study to evaluate the safety and effectiveness of FemPulse System
Official title: Evaluation of a Non-Implanted Electrical Stimulation Device for Overactive Bladder (OAB) EVANESCE-II
Key Details
Gender
FEMALE
Age Range
21 Years - Any
Study Type
INTERVENTIONAL
Enrollment
151
Start Date
2025-09-30
Completion Date
2027-12-31
Last Updated
2026-02-06
Healthy Volunteers
No
Conditions
Interventions
Device Group
non-implanted, vaginal electrical stimulation device
Medication Group
OAB Medication
Locations (15)
Cedars Sinai
Beverly Hills, California, United States
UCLA
Los Angeles, California, United States
UC Irvine
Orange, California, United States
Stanford
Palo Alto, California, United States
USCD
San Diego, California, United States
Holy Cross Medical Group - Women's Center
Fort Lauderdale, Florida, United States
Comprehensive Urologic
Barrington, Illinois, United States
University of Louisville
Louisville, Kentucky, United States
Chesapeake Urology
Owings Mills, Maryland, United States
Minnesota Urology
Woodbury, Minnesota, United States
Adult & Pediatric Urology
Omaha, Nebraska, United States
Atrium Health
Charlotte, North Carolina, United States
Southern Urogynecology
West Columbia, South Carolina, United States
Sanford Health
Sioux Falls, South Dakota, United States
INOVA
Falls Church, Virginia, United States