Polypropylene Mesh in Prolapse Surgery

Completed

• Conditions: Pelvic Organ Prolapse

• Registration Number: NCT02383199
• Lead Sponsor: Turku University Hospital

Brief Summary

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2013-09
• Primary Completion: 2014-06
• Study Completion: 2014-11
• Study First Submitted: 2015-02-02
• Status Verified: 2015-03
• Study First Submitted QC: 2015-03-03
• Study First Posted: 2015-03-09
• Last Update Submitted: 2015-03-26
• Last Update Posted: 2015-03-27

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 161

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Subjective outcome with validated questionnaires	7 years	Validated questionnaires

Secondary Outcome Measures

Name	Time	Method
Objective outcome: anatomic outcome with Pelvic Organ Prolapse Quantification (POP-Q) system	7 years
Number of patients with adverse events and reoperations.	7 years	POP-Q