Prospective Analysis of Restorelle in the Treatment of Uterine Prolapse

Status Active, not recruiting

Clinical Trial Summary

The purpose of this study is to determine the long term performance of Restorelle system for the treatment of uterine prolapse.

Clinical Trial Description

This study is being done to evaluate the performance of the Restorelle system, which uses Smartmesh - an ultra-lightweight mesh for uterine prolapse management. Most patients undergo a hysterectomy i.e. removal of the uterus when they have a prolapse. However, this has often been found to be an unnecessary operation. The investigators are studying the use of the Restorelle mesh system to preserve the uterus when there is a uterine prolapse. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02921451
Study type	Interventional
Source	Michigan Institution of Women's Health PC
Contact
Status	Active, not recruiting
Phase	N/A
Start date	August 2016
Completion date	August 2020

View Details

See also
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