Surgical Outcomes of Vaginal Prolapse Repair With Elevate
This trial is active, not recruiting.
|Start date||August 2010|
|End date||December 2016|
|Trial size||100 participants|
|Trial identifier||NCT01190618, 2010-176|
The purpose of this study is to evaluate outcomes in patients having vaginal prolapse repair with the Elevate prolapse repair kit and compare these outcomes to patients who had a repair with Prolift. .
Comparison of Outcomes
time frame: 3 Months
Female participants of any age.
Inclusion Criteria: - Women who have had a vaginal repair with Elevate prolapse repair kit Exclusion Criteria:
|Official title||Surgical Outcomes of Vaginal Prolapse Repair With the Elevate Prolapse Repair Kit|
|Principal investigator||Larry Sirls, MD|
|Description||The investigators hypothesize that the less invasive Elevate mesh results in a shorter operative time, lower blood loss, complications, postoperative pain and earlier discharge from the hospital.|
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