Kineflex|C Artificial Disc System to Treat Cervical Degenerative Disc Disease (DDD)
|ClinicalTrials.gov Identifier: NCT00374413|
Recruitment Status : Terminated (Economic and business factors)
First Posted : September 11, 2006
Last Update Posted : September 13, 2013
Information provided by (Responsible Party):
No Study Results Posted on ClinicalTrials.gov for this Study
|Recruitment Status :||Terminated|
|Actual Primary Completion Date :||January 2010|
|Actual Study Completion Date :||August 2013|
|Certification/Extension First Submitted :||July 19, 2011|
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Coric D, Guyer RD, Nunley PD, Musante D, Carmody C, Gordon C, Lauryssen C, Boltes MO, Ohnmeiss DD. Prospective, randomized multicenter study of cervical arthroplasty versus anterior cervical discectomy and fusion: 5-year results with a metal-on-metal artificial disc. J Neurosurg Spine. 2018 Mar;28(3):252-261. doi: 10.3171/2017.5.SPINE16824. Epub 2018 Jan 5.
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. Epub 2011 Jun 24. Erratum in: J Neurosurg Spine. 2012 Mar;16(3):322.