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.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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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
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Locations
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CH La Rochelle
La Rochelle, 17019, France
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CH de Saintonge
Saintes, 17108, France
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CHU Pellegrin
Bordeaux, 33076, France
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Clinique Bon Secours
Le Puy-en-Velay, 43000, France
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Institut Mutualiste Montsouris
Paris, 75014, France
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Polyclinique de la Baie
Avranches, Choisir Une Région, 50300, France