Trials / Completed
CompletedNCT03281564
Quality of Life After Laparoscopic Removal of Essure®
Prospective Study of Quality of Life After Laparoscopic Removal of Essure®
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 474 (actual)
- Sponsor
- Hospices Civils de Lyon · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
A lot of patients seem to complain after hysteroscopic tubal occlusion by Essure® device with a worce quality of life. Investigators' hypothesis is that Essure® laparoscopic removal may improve quality of life. This prospectice study aim to assess the quality of life 1, 3, 6 and 12 months after Essure® removal.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Quality of life after Essure® removal | Questionnaire to assess the quality of life 1, 3, 6 and 12 months after laparoscopic removal of Essure® device |
Timeline
- Start date
- 2017-10-14
- Primary completion
- 2023-10-17
- Completion
- 2023-10-17
- First posted
- 2017-09-13
- Last updated
- 2023-11-13
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT03281564. Inclusion in this directory is not an endorsement.