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Clinical Trials/NCT05683041
NCT05683041
Recruiting
Not Applicable

Prevention of Intra-uterine Adhesions Following Laparoscopic and Laparotomic Myomectomy

University Hospital, Ghent1 site in 1 country30 target enrollmentFebruary 22, 2023
ConditionsMyoma

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Myoma
Sponsor
University Hospital, Ghent
Enrollment
30
Locations
1
Primary Endpoint
Adhesion formation postoperatief.
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

Clinical study on the prevention of intrauterine adhesions after laparoscopic or laparotomic myomectomy.

Myomas are common in women of reproductive age and myomectomy can lead to intra-uterine adhesions, which can be detrimental to fertility. This study investigates whether the use of an intrauterine gel can prevent the development of these adhesions.

Detailed Description

Design: Double-blind, randomized controlled pilot trial. Participant: * age between 18 and 45 years. * intramurale and/or subserosal myoma (FIGO 3-6), and/or hybrid myoma (with a connection to the endometrium and serosa (FIGO 2-5), who are scheduled for laparoscopic / laparotomic myomectomy. * absence of intra-uterine adhesions on preoperative diagnostic hysteroscopy Treatment: Application of intrauterine Hyalobarrier® gel endo at time of surgery Control: No application of Hyalobarrier® gel endo Follow up: Second-look hysteroscopy after 3months To blind all trial participants and gynaecologists doing second-look hysteroscopy, 10 ml of a sterile ultrasound gel will be applied into the vagina at the end of the procedure in all women regardless of their treatment allocation.

Registry
clinicaltrials.gov
Start Date
February 22, 2023
End Date
January 2028
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • age between 18 and 45 years.
  • intramurale and/or subserosal myoma (FIGO 3-6), and/or hybrid myoma (with a connection to the endometrium and serosa (FIGO 2-5), who are scheduled for laparoscopic / laparotomic myomectomy.
  • absence of intra-uterine adhesions on preoperative diagnostic hysteroscopy

Exclusion Criteria

  • pregnancy.
  • laparoscopic or laparotomic myomectomy in combination with an operative hysteroscopy.
  • presence of endometritis.
  • other antiadhesion methods

Outcomes

Primary Outcomes

Adhesion formation postoperatief.

Time Frame: 3 months post surgery

The presence of intra-uterine adhesions on a second look hysteroscopy.

Secondary Outcomes

  • Severity of adhesion formation(3 months post surgery, at the time of the hysteroscopy.)

Study Sites (1)

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