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ISASS: Use of ACADIA device for lumbar spinal stenosis improves pain and function
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ISASS: Use of ACADIA device for lumbar spinal stenosis improves pain and function

Contributing Authors

AD Tahernia JJ Regan T Briggs MP Lorio J Youssef S Webb D Whiting K Baker J Myer

161 patients were randomized in this Investigational Device Exemption (IDE) study to assess the safety and efficacy of the ACADIA Facet Replacement System for lumbar spinal stenosis. Patients received either the ACADIA device or instrumented posterolateral fusion (PLF) and were assessed after 36 months. Results revealed that the ACADIA device led to similar improvements as posterolateral fusion regarding symptoms, physical function, and back and leg pain.

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OrthoEvidence. ISASS: Use of ACADIA device for lumbar spinal stenosis improves pain and function. ACE Report. 2013;3(4):101. Available from: https://myorthoevidence.com/AceReport/Report/

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