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TDR: Safety and favourable outcomes obersved with Kineflex|C artificial disc
November 2013
TDR: Safety and favourable outcomes obersved with Kineflex|C artificial disc
Study Type:Therapy
OE Level Evidence:2
Journal Level of Evidence:N/A
Prospective, randomized, multicenter study of cervical arthroplasty: 269 patients from the Kineflex|C artificial disc investigational device exemption study with a minimum 2-year follow-up: clinical article
J Neurosurg Spine. 2011 Oct;15(4):348-58. doi: 10.3171/2011.5.SPINE10769. Epub 2011 Jun 24Did you know you're eligible to earn 0.5 CME credits for reading this report? Click Here
Synopsis
269 patients were randomized to determine the efficacy and safety of cervical arthroplasty with the Kineflex|C artificial disc in treatment of cervical radiculopathy. Patients were allocated to receive either cervical total disc replacement with the Kineflex|C cervical disc or anterior cervical discectomy and fusion, and were followed-up for a minimum of 24 months. Results at 24 month follow-up in...
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