Post-Approval Study Protocol for the Simplify Cervical Artificial Disc
Condition: Cervical Degenerative Disc Disorder · Sponsor: NuVasive
About this study
This study is intended to demonstrate the 5-year long-term safety and efficacy of the Simplify® Cervical Artificial Disc ("Simplify Disc") in subjects enrolled in the non-randomized Simplify Disc IDE study. This study was conducted under IDE G140154.
This description comes directly from the study's public registry record.
Talk to the study team
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
Locations (15)
| Orthopaedic Education and Research Institute of Southern California | Orange, California, United States | — |
| USCD | San Diego, California, United States | — |
| The Spine Institute for Spine Restoration | Santa Monica, California, United States | — |
| Spine Education and Research Foundation | Thornton, Colorado, 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 | — |
| Orthopaedic Institute of Western Kentucky | Paducah, Kentucky, United States | — |
| Spine institute of Louisiana | Shreveport, Louisiana, United States | — |
| Rothman Institute | Egg Harbor, New Jersey, United States | — |
| Buffalo Spine Surgery | Lockport, New York, United States | — |
| Carolina Neurosurgery and Spine Associates | Charlotte, North Carolina, United States | — |
+ 3 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT04630626