Cervical Interbody Implant Study
NCT04689854 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 150
Last updated 2025-12-22
Summary
The primary objective of this study is to evaluate the safety and performance of cervical spine surgery using interbody implants as measured by reported complications, radiographic outcomes, and patient-reported outcomes (PROs).
Conditions
- Degenerative Disc Disease
- Cervical Spinal Instability
Sponsors & Collaborators
-
NuVasive
lead INDUSTRY
Principal Investigators
-
Kyle Malone, MS · Globus Medical
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-07-07
- Primary Completion
- 2025-12-31
- Completion
- 2025-12-31
Countries
- United States
Study Locations
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