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Clinical Trial Summary

PREVENDO is a prospective, multicenter, pilot, and randomized study in 2 parallel arms and single blind, evaluating the proportion of endometrial synechiae 6 weeks after surgery in patients undergoing abdominal myomectomy or polymyomectomy, according to the application or not of an anti-adhesion gel (HYALOBARRIER® GEL ENDO)


Clinical Trial Description

Myomas are a common pathology affecting a large population of women of reproductive age. Depending on their location and the patient's symptoms, surgical removal of fibroids may be indicated. Interstitial or subserous myomas are accessible through the abdominal route (laparotomy or minimally invasive surgery). The impact of this surgery on the endometrial cavity and the risk of post-surgery synechiae is poorly understood, although it is essential, especially in a population of women wishing to preserve their fertility. In order to reduce and prevent endometrial synechia formation, we suggest PREVENDO study which consist in the systematic intracavitary placement of an anti-adhesion gel (HYALOBARRIER® GEL ENDO) immediately after surgery in patients undergoing abdominal myomectomy or polymyomectomy (laparotomy, laparoscopy, robot-assisted laparoscopy) and the evaluation of the proportion of endometrial synechiae 6 weeks after surgery in patients during diagnostic hysteroscopy performed 6 weeks after surgery. ;


Study Design


Related Conditions & MeSH terms

  • Patients With an Indication for Myomectomy or Polymyomectomy

NCT number NCT04702399
Study type Interventional
Source Assistance Publique - Hôpitaux de Paris
Contact Geoffroy Doctor CANLORBE
Phone 01 42 17 81 11
Email geoffroy.canlorbe@aphp.fr
Status Not yet recruiting
Phase N/A
Start date February 1, 2021
Completion date May 1, 2022