Post-Approval Study Protocol for the Simplify Cervical Artificial Disc

Completed · Not applicable

Conditions studied: Cervical Degenerative Disc Disorder

In brief

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.

Key facts

Study ID
NCT04630626
Run by
NuVasive
People needed
145
Starts
2021-01-01
Expected to finish
2023-04-23
Last updated by the study team
2026-01-08

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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