CompletedNot Applicable

Quality of Life Assessment Before and After Essure Removal

France95 participantsStarted 2017-01-10

Plain-language summary

To evaluate quality of life before and after laparoscopic removal of the Essure® system. Women who complain about symptoms attributed to the Essure® device are expected to have an improved quality of life postoperatively.

Who can participate

Age range18 Years

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients carrying Essure® * Patients requesting surgical removal of Essure® * Patients with adverse effect * Being affiliated or benefiting from a French social security system Exclusion Criteria: \- Patients with guardianship or curators

What they're measuring

Improving the quality of life between pre and post-operative at 3 months

Timeframe: 3 months after the surgery

Trial details

NCT IDNCT03401437

SponsorUniversity Hospital, Montpellier

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2018-01-31

View on ClinicalTrials.gov More Patients Presenting Essure Device Attributed Symptoms trials