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AccuLIF® PROSPECTIVE PATIENT OUTCOMES STUDY — APROPOS  

Degenerative Disc Disease Clinical Trial

Official title:
A Prospective Multi-Center Evaluation of a Hydraulic Expandable TLIF Cage for the Treatment of Degenerative Disc Disease of the Lumbar Spine

Clinical Trial Summary

This is a post-market clinical study of the AccuLIF expandable transforaminal lumbar interbody fusion (TLIF) cage in patients requiring surgery for degenerative disc disease (DDD) with up to Grade I spondylolisthesis or retrolisthesis, at one or two levels, between L2 and S1.

Clinical Trial Description

Study evaluations will be evaluated pre-operatively and at 6-weeks, 3-months, 6-months, 12-months and 24-months post-operatively to assess clinical outcomes, patient reported outcomes and radiographic status. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02704689
Study type Interventional
Source Stryker Spine
Contact
Status Terminated
Phase N/A
Start date June 8, 2016
Completion date January 19, 2017
View Details
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