Kineflex|C Artificial Disc System to Treat Cervical Degenerative Disc Disease (DDD)
This study has been terminated.
(Economic and business factors)
Information provided by (Responsible Party):
First received: September 7, 2006
Last updated: August 31, 2013
Last verified: August 2013
No Study Results Posted on ClinicalTrials.gov for this Study
|Study Status:||This study has been terminated.|
|Study Completion Date:||August 2013|
|Primary Completion Date:||January 2010 (Final data collection date for primary outcome measure)|
|Certification or Request for Extension to Delay Results Received:||July 19, 2011|
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Coric D, Nunley PD, Guyer RD, Musante D, Carmody CN, Gordon CR, Lauryssen C, Ohnmeiss DD, Boltes MO. 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. Erratum in: J Neurosurg Spine. 2012 Mar;16(3):322.