Surgical Outcomes of Vaginal Prolapse Repair With Elevate

NCT ID: NCT01190618

Last Updated: 2017-02-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

417 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-08-31

Study Completion Date

2016-12-31

Brief Summary

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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

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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.

Conditions

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Vaginal Prolapse

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

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

Exclusion Criteria

* N/A
Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Larry Sirls

OTHER

Sponsor Role lead

Responsible Party

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Larry Sirls

Principal Investigator

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Larry Sirls, MD

Role: PRINCIPAL_INVESTIGATOR

William Beaumont Hospitals

Locations

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William Beaumont Hospital

Royal Oak, Michigan, United States

Site Status

Countries

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United States

Other Identifiers

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2010-176

Identifier Type: -

Identifier Source: org_study_id

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