NCT04001426View on ClinicalTrials.gov

Pilot Phase for an Acute Evaluation of a Non-Implantable Electrical Continence Device

NACompletedINTERVENTIONAL
Enrollment

2

Participants

Timeline

Start Date

April 4, 2019

Primary Completion Date

December 31, 2019

Study Completion Date

December 31, 2019

Conditions
Urinary Bladder, Overactive
Interventions
DEVICE

The FemPulse System

Non-invasive monitoring during activation of the FemPulse System

Trial Locations (1)

55404

Hennepin Healthcare, Minneapolis

Sponsors
All Listed Sponsors
lead

FemPulse Corporation

INDUSTRY