Status:
COMPLETED
Comparison of 2 Lightweight Y-meshes After Laparoscopic Sacrocolpopexy
Lead Sponsor:
Atlantic Health System
Conditions:
Pelvic Organ Prolapse
Eligibility:
FEMALE
Brief Summary
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 lightwe...
Eligibility Criteria
Inclusion
- All patients who underwent robotic-assisted laparoscopic sacrocolpopexy between January 2007 to August 2011 using either Alyte Y-mesh or Restorelle Y-mesh
Exclusion
- Refusal to participate in our long-term outcome study
Key Trial Info
Start Date :
July 1 2014
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
August 1 2015
Estimated Enrollment :
316 Patients enrolled
Trial Details
Trial ID
NCT02248935
Start Date
July 1 2014
End Date
August 1 2015
Last Update
June 9 2017
Active Locations (1)
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1
Department of Urogynecology-Atlantic Health System
Morristown, New Jersey, United States, 07960