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Axis™ Allograft Dermis for Female Pelvic Floor Repair: a Prospective Post Market Study

Pelvic Organ Prolapse Clinical Trial

Official title:
Axis™ Allograft Dermis for Female Pelvic Floor Repair: a Prospective Post Market Study

Clinical Trial Summary

This study is a prospective, single arm, multi-center, post-market study to evaluate the efficacy of Axis™ Allograft Dermis used for anterior, posterior or combined (anterior and posterior) pelvic organ prolapse repair.

Clinical Trial Description

The study population will be adult female patients with pelvic organ prolapse, POP-Q Stage ≥ 2 that are clinically indicated for surgical intervention with Axis Allograft Dermis in the anterior, posterior or combined (anterior and posterior) compartments. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01541748
Study type Observational
Source Coloplast A/S
Contact
Status Completed
Phase
Start date November 2011
Completion date November 11, 2018
View Details
See also
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