Polypropylene Mesh in Prolapse Surgery

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.

Completed

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Key information

Conditions

Pelvic Organ Prolapse Pathological Conditions, Anatomical Pathological Conditions, Signs and Symptoms Prolapse

Sex eligibility

Female

Study type

Observational

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

Subjective outcome with validated questionnaires

Time frame: 7 years

Validated questionnaires

Secondary outcomes

Objective outcome: anatomic outcome with Pelvic Organ Prolapse Quantification (POP-Q) system

Time frame: 7 years
Number of patients with adverse events and reoperations.

Time frame: 7 years

POP-Q

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Completed

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Sponsors and collaborators

Lead sponsor

Turku University Hospital

Other Gov

Registry information

Official study title

Polypropylene Mesh in Prolapse Surgery; Long-term Outcome and Complications.

Important dates

Study start: 2013
Primary completion: 2014
Study completion: 2014
First posted: Mar 9, 2015
Registry last updated: Mar 27, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed