NCT00388947View on ClinicalTrials.gov

Observational Data Collection of Surgical Outcomes in the Treatment of Vaginal Prolapse With AMS Products

CompletedOBSERVATIONAL

Enrollment

1,543

Participants

Timeline

Start Date

September 30, 2006

Primary Completion Date

May 31, 2010

Study Completion Date

May 31, 2010

Conditions

Vaginal Prolapse

Interventions

DEVICE

AMS Prolapse Product

AMS Apogee™ with IntePro (Synthetic) or InteXen (Biologic) Mesh implant for posterior wall pelvic organ prolapse AMS Straight-In™ with IntePro (Synthetic) Mesh implant for vaginal vault pelvic organ prolapse AMS Perigee™ with IntePro Mesh implant for anterior wall pelvic organ prolapse AMS Perigee™ with IntePro Mesh coated with PC AMS Elevate® Prolapse Repair System Family

Trial Locations (1)

01588

Samuel Zylstra, MD, Whitinsville