This trial has been completed.

Condition vaginal prolapse
Sponsor Larry Sirls
Start date August 2010
End date December 2016
Trial size 417 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. .

United States No locations recruiting
Other countries No locations recruiting

Study Design

Observational model case-only
Time perspective retrospective

Primary Outcomes

Comparison of Outcomes
time frame: 3 Months

Eligibility Criteria

Female participants of any age.

Inclusion Criteria: - Women who have had a vaginal repair with Elevate prolapse repair kit Exclusion Criteria:

Additional Information

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.
Trial information was received from ClinicalTrials.gov and was last updated in February 2017.
Information provided to ClinicalTrials.gov by William Beaumont Hospitals.