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Restorelle® Mesh Versus Native Tissue Repair for Prolapse

Pelvic Organ Prolapse Clinical Trial

Official title:
Restorelle® Transvaginal Mesh Versus Native Tissue Repair for Treatment of Pelvic Organ Prolapse, Restorelle 522 Study

Clinical Trial Summary

The purpose of this study is to collect information on the safety and effectiveness of Restorelle Direct Fix mesh and the surgical procedure to implant Restorelle. These results will be compared to the safety and effectiveness results in patients who have native tissue repair (without mesh) as their pelvic organ prolapse treatment.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02162615
Study type Observational
Source Coloplast A/S
Contact
Status Completed
Phase
Start date August 2014
Completion date November 6, 2021
View Details
See also
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