Comparison of 2 Lightweight Y-meshes After Laparoscopic Sacrocolpopexy

Atlantic Health System

Status: Completed

Conditions: Pelvic Organ Prolapse

Study type: Observational

Funder types: Other

Identifiers

NCT02248935

599819-2

Details and patient eligibility

About

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.

Enrollment: 316 patients

Sex: Female

Volunteers: No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

• Refusal to participate in our long-term outcome study

Trial design

316 participants in 1 patient group

Repair with Alyte or Restorelle Y-Mesh

Description:

Women who underwent their index robotic-assisted laparoscopic sacrocolpopexy at Morristown Medical Center or Overlook Medical Center using either the Alyte Y-mesh or Restorelle Y-smartmesh between 1/2007 and 8/2011.