A Large Multi-Center Database of Women Who Have Had and Are Going to Have Surgical Correction of Their Pelvic Organ Prolapse Using the Gynecare Prolift System

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

Study Classification

OBSERVATIONAL

Study Start Date

2008-01-31

Study Completion Date

2009-12-31

Brief Summary

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retrospective and prospective data collection for a database. Patients will have had or are going to have a repair of their pelvic organ prolapse using the Gynecare mesh Prolift System

Detailed Description

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Conditions

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Pelvic Organ Prolapse

Keywords

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Gynecare Prolift Pelvic organ prolapse forming a large database of women who have recieve Gynecare prolift system

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Eligibility Criteria

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Inclusion Criteria

* women recieving surgery for their pelvic organ prolapse using the Gynecare mesh kit called Prolift

Exclusion Criteria

* none

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Responsible Party

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Institute for Female Pelvic Medicine

Locations

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Institute for Female Pelvic Medicine and Reconstructive Surgery

Allentown, Pennsylvania, United States

Site Status

Countries

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United States

Other Identifiers

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SLHN 2007-98

Identifier Type: -

Identifier Source: org_study_id