U.S., Sept. 30 -- ClinicalTrials.gov registry received information related to the study (NCT07195656) titled 'Evaluation of a Non-Implanted Electrical Stimulation Device for Overactive Bladder (OAB)' on Sept. 24.

Brief Summary: A study to evaluate the safety and effectiveness of FemPulse System

Study Start Date: Sept. 30

Study Type: INTERVENTIONAL

Condition: Overactive Bladder (OAB)

Intervention: DEVICE: Device Group

non-implanted, vaginal electrical stimulation device

DRUG: Medication Group

OAB Medication

Recruitment Status: NOT_YET_RECRUITING

Sponsor: FemPulse Corporation

Disclaimer: Curated by HT Syndication....