Performance and Safety of the PHENIX LIBERTY, a Medical Device for Electrostimulation and Biofeedback, in the Treatment of Pelvic Static Disorders in Women With Urinary Incontinence.

NACompletedINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

May 6, 2024

Primary Completion Date

December 6, 2024

Study Completion Date

December 6, 2024

Conditions
Urinary IncontinencePelvic Floor Disorders
Interventions
DEVICE

Electrical stimulation and biofeedback with the medical device Phenix Liberty

"The patient will undergo 10 therapeutic functional re-education sessions, at regular intervals according to a schedule drawn up by the physiotherapist, during which the PHENIX LIBERTY device may be used.~The patients will complete questionnaires at the end of the care Overall, the functional perineal rehabilitation sessions will include muscle testing, electrostimulation and biofeedback.~The follow up will be conduct as follow :~* 10 sessions between 10 and 12 weeks~* 1 end visit, within the week after the 10th session"

Trial Locations (2)

30000

Human Physio, Nîmes

06370

Pôle santé de la Nartassière, Mouans-Sartoux

All Listed Sponsors
collaborator

CEISO

INDUSTRY

collaborator

Human Physio

UNKNOWN

collaborator

Pôle santé de la Nartassière

UNKNOWN

lead

Vivaltis

INDUSTRY

NCT05938855 - Performance and Safety of the PHENIX LIBERTY, a Medical Device for Electrostimulation and Biofeedback, in the Treatment of Pelvic Static Disorders in Women With Urinary Incontinence. | Biotech Hunter | Biotech Hunter