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....