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Prospective study of disc repair with allogeneic chondrocytes presented at the 2012 Joint Spine Section Meeting.
OBJECT The purpose of the study was to evaluate the safety and initial efficacy of NuQu allogeneic juvenile chondrocytes delivered percutaneously for the treatment of lumbar spondylosis with… Expand
Clinical and Radiographic Outcome of the NeoDisc Cervical Total Disc Replacement (TDR) at 2-Year Follow-up
- Kenneth Pettine
- 1 September 2010
A Phase II Study Demonstrating Efficacy and Safety of Mesenchymal Precursor Cells in Low Back Pain Due to Disc Degeneration
22. Why Lumbar Artificial Disc Replacements (ADR) Fail: Home Run or Strike Out?
Five-Year Follow-Up of a Prospective, Randomized Trial Comparing Two Lumbar Total Disc Replacements
Study Design. This was a prospective, randomized, controlled, multicenter study. Objective. The purpose of this study was to compare outcomes of two lumbar total disc replacements (TDRs) at 5-year… Expand
Comparison of 2 Lumbar Total Disc Replacements: Results of a Prospective, Randomized, Controlled, Multicenter Food and Drug Administration Trial With 24-Month Follow-up
Study Design. This was a prospective, randomized, controlled multicenter study with 24-month follow-up. Objective. The purpose of this study was to evaluate the safety and efficacy in a Food and Drug… Expand
Kineflex lumbar artificial disc versus Charité lumbar total disc replacement for the treatment of degenerative disc disease: A randomized non-inferiority trial with minimum of 2 years’ follow-up
Background The Kineflex lumbar artificial disc replacement device (SpinalMotion, Mountain View, California) is a semiconstrained, posterior center of rotation, metal-on-metal intervertebral disc… Expand
P5. A Prospective Randomized Comparison of Two Lumbar Total Disc Replacements: Results at 24-Month Follow-Up
Prestige ST Cervical Artificial Disc Results with Up to Three-Year Follow-Up
- Kenneth Pettine
- 1 September 2013