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A Pilot Study to Investigate the Efficacy of Partially Absorbable Mesh in Patients With Pelvic Organ Prolapsed

Pelvic Organ Prolapse Clinical Trial

Official title:
A Prospective Pilot Study to Investigate the Efficacy of Partially Absorbable Mesh(Seratom PA®) in Patients With Pelvic Organ Prolapsed

Clinical Trial Summary

The purpose of this study is to evaluate the efficacy, recurrence, postoperative complications of partially absorbable mesh(Seratom®PA) in patients with pelvic organ prolapse.

Clinical Trial Description

Patients with pelvic organ prolapse are administrated partially absorbable mesh(Seratom®PA). It is performed pelvic organ prolapse quantification(POP-Q) examination, quality of life(QOL) questionnaire complications at postop 2week, 12week, 24week. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02320643
Study type Interventional
Source Samyang Biopharmaceuticals Corporation
Contact
Status Completed
Phase N/A
Start date December 2014
Completion date April 2017
View Details
See also
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