Temporary ovarian suspension during laparoscopy to reduce postoperative adhesions

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This prospective, single-blinded randomized controlled trial enrolls patients with moderate-to-severe endometriosis who are at risk for ovarian adhesions and randomizes them to laparoscopic surgery with temporary ovarian suspension or to standard care without suspension. Participants complete daily questionnaires about pain and suture removal eagerness after surgery. Blinded ultrasound experts evaluate adhesion formation at about 6 and 13 weeks postoperatively, and no anti-adhesive barriers are used to reduce confounding. The trial compares adhesion rates and early postoperative symptoms between the two groups.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patients with moderate to severe endometriosis with suspected adhesions, lesions in the ovary, ovarian fossa, utero-sacral ligaments, pouch of douglas, or involvement of the intestine as seen in preoperative assessment who are willing to participate in the study including postoperative follow-up assessments.

Exclusion Criteria:

* Patients who are not intended to have an endometriosis operation. Patients with minimal to mild endometriosis and no suspected adhesions or ovarian, ovarian fossa, utero-sacral ligament, pouch of douglas involvement on preoperative assessment.

Where it's running

• Carmel Medical Center
  Haifa, Israel Recruiting

Study contacts

• Study coordinator: Yuval Kaufman, MD
• Email: mdykaufman@gmail.com
• Phone: +97248250336

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.