Viewing Study NCT01190618


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Study NCT ID: NCT01190618
Status: COMPLETED
Last Update Posted: 2017-02-16
First Post: 2010-08-26
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Surgical Outcomes of Vaginal Prolapse Repair With Elevate
Sponsor: Larry Sirls
Organization:

Study Overview

Official Title: Surgical Outcomes of Vaginal Prolapse Repair With the Elevate Prolapse Repair Kit
Status: COMPLETED
Status Verified Date: 2017-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: 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. .
Detailed 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.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: