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Clinical Trial Summary

Our study is a non-randomized prospective study compared two groups matched for anterior/apical POP-Q grade: 84 received Elevate Ant™ single-incision mesh (group A) and 42 Perigee™ transvaginal mesh (group B). The study hypothesis was that the Elevate Ant™ mesh would provide better apical correction than the Perigee™ mesh. One- and 2-year follow-up comprised anatomic assessment (POP-Q) and QoL (PFDI-20, PFIQ-7, PISQ-12). Success was defined as 2-year POP-Q ≤1. Secondary endpoints were function and complications.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03187574
Study type Observational
Source Hospices Civils de Lyon
Contact
Status Completed
Phase N/A
Start date May 2009
Completion date April 2016

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