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Approval Date: 8/24/2010
Principal Investigator: Larry Sirls, MD
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. 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.
For more information visit http://ClinicalTrials.gov/show/NCT01190618
Kim Killinger, Research Coordinator
Status of Clinical Trial: open and enrolling