Mesh study follows patients for years after prolapse surgery
NCT ID NCT06296316
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study followed 39 women who had surgery for pelvic organ prolapse using Restorelle mesh. The goal was to track safety and how well the mesh worked over 5 to 8 years after surgery. No new treatment was given—just routine check-ups to see if any further surgery was needed.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
39 people
The number who actually took part.
- Started
-
Nov 2023
- Finished
-
Nov 2024
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult female patients presenting with apical pelvic organ prolapse which is clinically indicated for a surgical treatment with Restorelle mesh
- Ages
-
18 years and older
- Sex
-
Female participants only
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Female patient of at least 18 years old * Patient presenting apical pelvic organ prolapse and being eligible to surgical treatment * Surgeon having decided to treat the patient with a Restorelle mesh as per its CE mark indication and IFU, before patient inclusion * Patient having received appropriate information and counselling before mesh implantation * Patient has been provided written informed consent Exclusion Criteria: * Patient currently pregnant or breastfeeding * Patient being deprived of liberty by a judicial or administrative decision, or who is under a measure of legal protection
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Genital prolapse are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
CH La Rochelle
La Rochelle, 17019, France
-
CH de Saintonge
Saintes, 17108, France
-
CHU Pellegrin
Bordeaux, 33076, France
-
Clinique Bon Secours
Le Puy-en-Velay, 43000, France
-
Institut Mutualiste Montsouris
Paris, 75014, France
-
Polyclinique de la Baie
Avranches, Choisir Une Région, 50300, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.