U.S., March 21 -- ClinicalTrials.gov registry received information related to the study (NCT06885099) titled 'Ease of Use Study of the FemPulse System' on Feb. 11.

Brief Summary: The objective of the study is to demonstrate that the FemPulse System can be used as indicated

Study Start Date: Feb. 11

Study Type: INTERVENTIONAL

Condition: Overactive Bladder (OAB)

Intervention: DEVICE: FemPulse System

Subjects to receive the FemPulse System consisting of a non-implanted, vaginal electrical stimulation device (Ring) and other patient accessories.

Recruitment Status: RECRUITING

Sponsor: FemPulse Corporation

Published by HT Digital Content Services with permission from Health Daily Digest....