Comparison of 2 Lightweight Y-meshes After Laparoscopic Sacrocolpopexy

NCT02248935 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 316

Last updated 2017-06-09

No results posted yet for this study

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

  • Pelvic Organ Prolapse

Sponsors & Collaborators

  • Atlantic Health System

    lead OTHER

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-07-31
Primary Completion
2015-08-31
Completion
2015-08-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02248935 on ClinicalTrials.gov