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....