Trials / Completed
CompletedNCT03985345
Prospective Evaluation of the Connected EMY Biofeedback Probe in the Management of Stress Urinary Incontinence.
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 55 (actual)
- Sponsor
- University Hospital, Strasbourg, France · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
After birth, the perineum has to be trained in order to recover its functions. This study is designed to assess the quality of life evolution with the EMY connected device. The secondary purposes are to evaluate patient compliance to the EMY probe, to observe the evolution of urine scores over the duration of the trial in order to consider a comparative study thereafter, and to evaluate the interest of using the EMY connected perineal probe in the context of stress urinary incontinence.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | intravaginal device (probe) EMY | Free use of EMY and its mobile application for 10 minutes during 5 different days per week. |
Timeline
- Start date
- 2019-09-02
- Primary completion
- 2020-09-09
- Completion
- 2020-09-09
- First posted
- 2019-06-13
- Last updated
- 2025-10-01
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT03985345. Inclusion in this directory is not an endorsement.