Investigation of the Two Level Simplify® Cervical Artificial Disc
Condition: Cervical Degenerative Disc Disorder · Sponsor: NuVasive
About this study
This study is intended to demonstrate that the Simplify® Cervical Artificial Disc (Simplify® Disc) is at least as safe and effective as conventional anterior cervical discectomy and fusion (ACDF) when used to treat two contiguous discs from C3 to C7 following discectomy at two contiguous levels for intractable radiculopathy (arm pain and/or a neurological deficit) with neck pain or myelopathy due to abnormalities localized to the levels of the two contiguous disc spaces in subjects who are unresponsive to conservative management.
This description comes directly from the study's public registry record.
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No contact information is available for this study as per the public registry record.
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Locations (18)
| Orthopaedic Education and Research Institute of Southern California | Orange, California, United States | — |
| The Spine Institute for Spine Restoration | Santa Monica, California, United States | — |
| Spine Education and Research Foundation | Thornton, Colorado, United States | — |
| Connecticut Orthopaedic Specialists | Hamden, Connecticut, United States | — |
| Kennedy-White orthopedic Center | Sarasota, Florida, United States | — |
| NorthShore University Health System | Evanston, Illinois, United States | — |
| Indiana Spine Group | Carmel, Indiana, United States | — |
| Parkview Research Center | Fort Wayne, Indiana, United States | — |
| Orthopaedic Institute of Western Kentucky | Paducah, Kentucky, United States | — |
| Spine institute of Louisiana | Shreveport, Louisiana, United States | — |
| William Beaumont Hospital | Royal Oak, Michigan, United States | — |
| Buffalo Spine Surgery | Lockport, New York, United States | — |
+ 6 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT03123549