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Polypropylene Mesh in Prolapse Surgery

NCT02383199 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 161

Last updated 2015-03-27

No results posted yet for this study

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.

Conditions

  • Pelvic Organ Prolapse

Sponsors & Collaborators

  • Turku University Hospital

    lead OTHER_GOV

Principal Investigators

  • Pia Heinonen, MD · Turku university hospital, Department of gynecology and obsteterics, Turku, Finland':'

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2014-06-30
Completion
2014-11-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02383199 on ClinicalTrials.gov