CompletedNot Applicable

Evaluation of the Avaulta Procedure for the Correction of Pelvic Organ Prolapse - Results at 1 Year

United States103 participantsStarted 2007-10

Plain-language 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.

Who can participate

Age range18 Years

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * All patiAll patients who underwent surgery with the Avaulta synthetic mesh kit from 1/06 - 4/08. Exclusion Criteria: * Unable to give informed consent to participate

What they're measuring

Anatomical success rates 1 year after surgery to correct pelvic organ prolapse with the Avaulta synthetic mesh kit

Timeframe: 1 year post operatively

Trial details

NCT IDNCT00774215

SponsorAtlantic Health System

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2009-04

View on ClinicalTrials.gov More Pelvic Organ Prolapse trials