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Quality of Life After Laparoscopic Removal of Essure®

NCT03281564 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 474

Last updated 2023-11-13

No results posted yet for this study

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

  • Contraceptive Device; Complications
  • Quality of Life

Interventions

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

Sponsors & Collaborators

  • Hospices Civils de Lyon

    lead OTHER

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-10-14
Primary Completion
2023-10-17
Completion
2023-10-17

Countries

  • France

Study Locations

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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 NCT03281564 on ClinicalTrials.gov