Clinical outcomes with selectively constrained SECURE-C cervical disc arthroplasty: two-year results from a prospective, randomized, controlled, multicenter investigational device exemption study.

@article{Vaccaro2013ClinicalOW,
  title={Clinical outcomes with selectively constrained SECURE-C cervical disc arthroplasty: two-year results from a prospective, randomized, controlled, multicenter investigational device exemption study.},
  author={Alexander R. Vaccaro and William Beutler and Walter C Peppelman and Joseph M Marzluff and Jason M Highsmith and Andrew S Mugglin and George E Demuth and Manasa Gudipally and Kelly J Baker},
  journal={Spine},
  year={2013},
  volume={38 26},
  pages={2227-39}
}
STUDY DESIGN Prospective, multicenter, randomized, and controlled Investigational Device Exemption clinical trial. OBJECTIVE To compare the clinical safety and effectiveness of the selectively constrained SECURE-C (Globus Medical, Audubon, PA) Cervical Artificial Disc to anterior cervical discectomy and fusion (ACDF). SUMMARY OF BACKGROUND DATA Cervical total disc replacement has been developed as an alternative to ACDF by allowing segmental motion. Current cervical total disc replacement… CONTINUE READING

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