Surgical Outcomes of Vaginal Prolapse Repair With Elevate

Surgical Outcomes of Vaginal Prolapse Repair With the Elevate Prolapse Repair Kit

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01190618

Enrollment

417

Registered

2010-08-27

Start date

2010-08-31

Completion date

2016-12-31

Last updated

2017-02-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Vaginal Prolapse

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.

Interventions

None listed

Study design

Observational model

CASE_ONLY

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Healthy volunteers

Inclusion criteria

* Women who have had a vaginal repair with Elevate prolapse repair kit

Exclusion criteria

* N/A

Design outcomes

Primary

Measure	Time frame	Description
Comparison of Outcomes	3 Months	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 Profift.

Countries

United States

Outcome results