Status:
COMPLETED
Evaluation of the Avaulta Procedure for the Correction of Pelvic Organ Prolapse - Results at 1 Year
Lead Sponsor:
Atlantic Health System
Conditions:
Pelvic Organ Prolapse
Eligibility:
FEMALE
18+ years
Brief Summary
This study is a 1 year review of all patients who had surgery to correct pelvic organ prolapse (i.e. cystocele, rectocele, enterocele) using the Avaulta synthetic mesh kit.
Detailed Description
This is a retrospective cohort analysis of all patients who experienced vaginal prolapse and were operated on with the Avaulta synthetic vaginal mesh "kit" from January 2006 to April 2007. The Avaulta...
Eligibility Criteria
Inclusion
- All patiAll patients who underwent surgery with the Avaulta synthetic mesh kit from 1/06 - 4/08.
Exclusion
- Unable to give informed consent to participate
Key Trial Info
Start Date :
October 1 2007
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
April 1 2009
Estimated Enrollment :
103 Patients enrolled
Trial Details
Trial ID
NCT00774215
Start Date
October 1 2007
End Date
April 1 2009
Last Update
January 26 2010
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Atlantic Health System - Division of Urogynecology
Morristown, New Jersey, United States, 07960