Trials / Completed
CompletedNCT02248935
Comparison of 2 Lightweight Y-meshes After Laparoscopic Sacrocolpopexy
Prospective Cohort Study Comparing Two Lightweight Y Meshes After Robotic-Assisted Laparoscopic Sacrocolpopexy Longterm Outcomes
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 316 (actual)
- Sponsor
- Atlantic Health System · Academic / Other
- Sex
- Female
- Age
- —
- Healthy volunteers
- Not accepted
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 lightweight mesh.
Conditions
Timeline
- Start date
- 2014-07-01
- Primary completion
- 2015-08-01
- Completion
- 2015-08-01
- First posted
- 2014-09-25
- Last updated
- 2017-06-09
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02248935. Inclusion in this directory is not an endorsement.