PREvention of Intrauterine Adhesion After Adhesiolysis With Novel Tri-block deGradable Polymer Film.
Condition(s) studied
Investigational drug(s) / intervention(s)
Womed Leaf: Womed Leaf™ device is composed of a uterine anti-adhesion film pre-loaded inside a flexible inserter. Womed Leaf™ is inserted in the uterine cavity by the gynecologist surgeon as a film folded into a 5 mm diameter flexible inserter. Once released, the film will unfold and swell into the uterine cavity to keep uterus walls separated. It is degraded and discharged naturally through the cervix and vagina.
Study summary
PREG2 is a randomized controlled trial that aims to evaluate efficacy in preventing intrauterine adhesion recurrence after hysteroscopic adhesiolysis of a novel intrauterine barrier film named Womed Leaf
Eligibility
Primary outcome measure(s)
- Efficacy - IUA Severity — At second look hysteroscopy between 4 and 8 weeks
Change of AFS score between pre-adhesiolysis and second-look hysteroscopy (AFS) score The scale used to assess the severity of intrauterine adhesions is the American Fertility Society score. It is a 12 points composite score that adds-up 3 subcomponents: - Extend of adhesions (1 = less than 1/3 of the uterine cavity involved with adhesions to 4 = more than 2/3 of the uterine cavity involved with adhesions), * Type of adhesions (1 = Filmy adhesions to 4 = dense adhesions) * Menstrual pattern (0= normal to 4 = amenorrhea). The final score allows the following prognostic classification: 1-4 = mild disease, 5-8 = moderate disease 9-12 = severe disease - Safety - Adverse Events — At second look hysteroscopy between 4 and 8 weeks
Adverse events up to second look hysteroscopy.
Trial sites (15)
| Facility | City | Region | Status |
|---|---|---|---|
| Gent UZ | Ghent | Belgium | |
| Guangdong Maternal and Child Health Hospital | Guangzhou | China | |
| Women's Hospital School Of Medicine Zhejiang University | Hangzhou | China | |
| The Obstetrics & Gynecology Hospital Affiliated to Fudan University | Shanghai | China | |
| Gynprenatal | Ostrava | Czechia | |
| CHU Bicêtre | Le Kremlin-Bicêtre | France | |
| CHU de Lille | Lille | France | |
| Hopital La Conception | Marseille | France | |
| CHU Lariboisière | Paris | France | |
| Clinique Mutualiste La sagesse | Rennes | France | |
| A.O.U Federico II | Naples | Italy | |
| Aso Mauriziano Umberto I | Torino | Italy | |
| Hospital Clinic Barcelonna | Barcelona | Spain | |
| Ramon y Cajal Hospital | Madrid | Spain | |
| Centre Hospitalier Universitaire Vaudois | Lausanne | Switzerland |
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04963179 on ClinicalTrials.gov ↗ ← All trials in Italy