Finished
Comparison of 2 Lightweight Y-meshes After Laparoscopic Sacrocolpopexy
NCT02248935 · Atlantic Health System · Updated 9 June 2017
- What is being tested
- Not stated
- For
- Pelvic Organ Prolapse
- Kind of study
- Watches patients without assigning a treatment. No drug phase (a device or procedure study).
- Who can join
- Ages Not stated. About 316 people. The full rules are on the registry page.
- Where
- United States
- When
- Starts or started July 2014, ends Aug 2015. Registered 25 Sept 2014.
- Results
- None posted yet.
In the researchers' words
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.
Sites
- Department of Urogynecology-Atlantic Health SystemMorristown, New Jersey, United States