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RECRUITING
NCT07195656
NA

Evaluation of a Non-Implanted Electrical Stimulation Device for Overactive Bladder (OAB)

Sponsor: FemPulse Corporation

View on ClinicalTrials.gov

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

Interventions

DEVICE

Device Group

non-implanted, vaginal electrical stimulation device

DRUG

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