Fenestrated Screw Study — FNS

Deformity of Spine Clinical Trial

Official title:
A Prospective, Multicenter Evaluation of the CD HORIZON® Fenestrated Screw Spinal System With Fenestrated Screw Cement When Used in the Treatment of Spinal Conditions in Subjects With Compromised Bone Quality

Status Terminated

Clinical Trial Summary

The primary objective of this post-market study is to demonstrate that Oswestry disability index (ODI) score improved significantly at 12 months post-operatively as compared to baseline for each indication (degenerative spinal disease and deformity) in subjects with compromised bone quality, who will receive a surgical procedure requiring posterior stabilization and/or immobilization of one or more spinal segments using CD HORIZON® Fenestrated Screw Spinal System with Fenestrated Screw Cement.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03797144
Study type	Interventional
Source	Medtronic Spinal and Biologics
Contact
Status	Terminated
Phase	N/A
Start date	April 18, 2019
Completion date	July 15, 2020

View Details

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