Polypropylene Mesh in Prolapse Surgery

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

161 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-09-30

Study Completion Date

2014-11-30

Brief Summary

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The purpose of this study was to report the long-term objective and subjective outcome after prolapse surgery with polypropylene mesh. The complications and the effect of the learning curve of the surgeons to the outcome is also reported.

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Detailed Description

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Conditions

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Pelvic Organ Prolapse

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

195 first patients with pelvic organ prolapse operated on using polypropylene mesh

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Pia Heinonen, MD

Role: PRINCIPAL_INVESTIGATOR

Turku university hospital, Department of gynecology and obsteterics, Turku, Finland':'

Other Identifiers

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134/2013

Identifier Type: -

Identifier Source: org_study_id

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