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Vaginal Uphold Hysteropexy and Laparoscopic Sacral Hysteropexy for the Treatment of Uterovaginal Pelvic Organ Prolapse — VAULT  

Pelvic Organ Prolapse Clinical Trial

Official title:
Vaginal Uphold Hysteropexy and Laparoscopic Sacral Hysteropexy for the Treatment of Uterovaginal Pelvic Organ Prolapse

Clinical Trial Summary

The purpose of this study is to evaluate surgical success or failure one year after surgery for pelvic organ prolapse.

Clinical Trial Description

This will be a prospective parallel cohort study comparing a laparoscopic sacral hysteropexy (LSHP) to a vaginal Uphold hysteropexy (VUHP). Symptomatic and anatomic improvement of pelvic organ prolapse will be evaluated at 3 months and 1 year. ;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01377142
Study type Observational
Source The Cleveland Clinic
Contact
Status Completed
Phase N/A
Start date June 2011
Completion date December 2015
View Details
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