NCT03985345View on ClinicalTrials.gov

Prospective Evaluation of the Connected EMY Biofeedback Probe in the Management of Stress Urinary Incontinence.

NACompletedINTERVENTIONAL
Enrollment

55

Participants

Timeline

Start Date

September 2, 2019

Primary Completion Date

September 9, 2020

Study Completion Date

September 9, 2020

Conditions
Stress Urinary Incontinence
Interventions
DEVICE

intravaginal device (probe) EMY

Free use of EMY and its mobile application for 10 minutes during 5 different days per week.

Trial Locations (1)

67091

Strasbourg University Hospitals, Strasbourg

All Listed Sponsors
collaborator

FIZIMED

UNKNOWN

lead

University Hospital, Strasbourg, France

OTHER

NCT03985345 - Prospective Evaluation of the Connected EMY Biofeedback Probe in the Management of Stress Urinary Incontinence. | Biotech Hunter | Biotech Hunter