CompletedNot Applicable

Ovariopexy for Adhesion Prevention After Laparoscopic Removal of Endometriosis of the Pelvic Side Wall or the Ovary

Germany409 participantsStarted 2018-04-01

Plain-language summary

prospective randomized Trial comparing ovariopexy over 2, 4 or 6 days vs Placebo after surgery because of endometriosis of the pelvic side wall or the ovary or both

Who can participate

Age range18 Years – 50 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: * premenopausal * wants to participate * removal of endometriosis of the pelvic side wall or ovary Exclusion Criteria: * postmenopausal * cannot give informed consent * no endometriosis during Operation * no Opening of pelvic side wall or ovary during the Operation * pregnant * breast feeding

What they're measuring

prevalence of postoperative ovarian adhesions

Timeframe: 3 months after operation

Trial details

NCT IDNCT04669756

SponsorUniversity Hospital Muenster

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2021-01-08

View on ClinicalTrials.gov More Endometriosis trials