Clinical Investigation to Assess a New Artificial Urinary Sphincter to Treat Urinary Incontinence in Women

NCT05828979 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 6

Last updated 2026-04-01

No results posted yet for this study

Summary

Prospective multicenter study designed to test the feasibility of the UroMems Artificial Urinary Sphincter in women

Conditions

  • Urinary Incontinence,Stress

Interventions

DEVICE

UroMems artificial urinary sphincter

Implantation of the device

Sponsors & Collaborators

  • UroMems SAS

    lead INDUSTRY

Principal Investigators

  • Emmanuel Chartier-Kastler · Groupe Hospitalier Pitié-Salpêtrière

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-05-02
Primary Completion
2025-01-23
Completion
2029-09-30

Countries

  • France

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05828979 on ClinicalTrials.gov