Early termination of study due to changes in funding.

This study is designed to compare the safety and efficacy of a commercially available mesh kit used for surgical repair of anterior vaginal wall prolapse with traditional suture repair surgery.

This is a multicenter, double blinded, randomized controlled trial, comparing Elevate® System with Interpro® Lite™, Anterior and Apical Prolapse Repair System (American Medical Systems) and Anterior Colporrhaphy (anterior suture repair) in women with symptomatic pelvic organ prolapse, who have opted to have surgical repair.

The goals of the study are to compare both efficacy and safety of the two procedures and to compare the surgical impact of mesh and suture repairs on vaginal function.

The principal investigator is from Mayo Clinic in Rochester, Minnesota. Mayo Clinic will serve as the data gathering and coordination site for this multicenter trial.

Inclusion Criteria:

• Women with symptomatic pelvic organ prolapse who opt for a vaginal repair
• Require both apical and anterior compartment repairs
• Willing to return for follow-up visit
• Understand and have signed informed consent to undergo randomization
• Need both an apical and anterior repair
• All trial participants who have a uterus will require a hysterectomy

Exclusion Criteria:

• Known or suspected vulvodynia
• Known or suspected interstitial cystitis
• History of chronic pelvic pain
• Current pregnancy
• Desire to maintain fertility
• History of reconstructive pelvic surgery with synthetic mesh
• History of radical pelvic surgery
• History of pelvic radiation therapy
• Currently undergoing treatment for a malignancy
• Medically poor candidates for surgery

5 women were enrolled at the German site (St. Hedwig's). No subjects were enrolled at the US sites.

Early termination of study due to changes in funding.