Comparison of 2 Lightweight Y-meshes After Laparoscopic Sacrocolpopexy

Completed

Conditions studied: Pelvic Organ Prolapse

In brief

The purpose of the study is to determine the clinical cure rates of pelvic organ prolapse from subjects that had a robotic-assisted sacrocolpopexy using Alyte Y mesh and Restorelle Y smartmesh lightweight mesh.

Key facts

Study ID

NCT02248935

Run by

Atlantic Health System

People needed

316

Starts

2014-07-01

Expected to finish

2015-08-01

Last updated by the study team

2017-06-09

Who can join

Age: any. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• All patients who underwent robotic-assisted laparoscopic sacrocolpopexy between January 2007 to August 2011 using either Alyte Y-mesh or Restorelle Y-mesh

You may not qualify if…

• Refusal to participate in our long-term outcome study

Where it is running

• Department of Urogynecology-Atlantic Health System — Morristown, New Jersey, United States

Full record on ClinicalTrials.gov

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