A Large Multi-Center Database of Women Who Have Had and Are Going to Have Surgical Correction of Their Pelvic Organ Prolapse Using the Gynecare Prolift System

Completed

• Conditions: Pelvic Organ Prolapse

• Registration Number: NCT01134003
• Lead Sponsor: The Institute of Pelvic Medicine & Reconstructive Surgery, Allentown, Pennsylvania

Brief Summary

retrospective and prospective data collection for a database. Patients will have had or are going to have a repair of their pelvic organ prolapse using the Gynecare mesh Prolift System

Detailed Description

Not available

Study Timeline

• Study Start: 2008-01
• Primary Completion: 2009-11
• Study Completion: 2009-12
• Status Verified: 2010-05
• Study First Submitted: 2010-05-27
• Study First Submitted QC: 2010-05-28
• Last Update Submitted: 2010-05-28
• Study First Posted: 2010-05-31
• Last Update Posted: 2010-05-31

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

• women recieving surgery for their pelvic organ prolapse using the Gynecare mesh kit called Prolift

Exclusion Criteria

• none

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Trial Locations

Locations (1)

Institute for Female Pelvic Medicine and Reconstructive Surgery; 🇺🇸 Allentown, Pennsylvania, United States