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Cervical Interbody Implant Study

StatusEnrolling by Invitation
PhaseNot specified
SponsorNuVasive
Started
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Record status
This record was last updated December 22, 2025 (before its estimated December 31, 2025 completion). Its status may not reflect the trial's current state.

Record History

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  1. Primary and study completion dates: Dec 31, 2024 to Dec 31, 2025v12
  2. Re-verified, no change to tracked fieldsv11
  3. Study sites: 6 to 7v10
  4. Re-verified, no change to tracked fieldsv9
  5. Study sites: 5 to 6v8
Show 6 earlier versionsHide 6 earlier versions
  1. Study sites: 4 to 5
    • Secondary endpoints: 4 to 7
    • Eligibility criteria shortened, about 2 words
    v7
  2. 2 versions Re-verified since Feb 16, 2022, no change to tracked fieldsv5-v6
  3. Study sites: 3 to 4v4
  4. Trial status: Not Yet Recruiting to Enrolling by Invitation
    • Study sites: 0 to 3
    • Start date changed from estimate of Feb 28, 2021 to Jul 7, 2020
    v3
  5. Start date: Dec 31, 2020 to Feb 28, 2021
    • Secondary endpoints revised (4)
    v2
  1. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
NuVasive
13 trials monitored
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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).
Trial Details
NCT Number NCT04689854
Lead Sponsor NuVasive
Conditions
(from sponsor)		 Degenerative Disc Disease, Cervical Spinal Instability
Related terms Intervertebral Disc Degeneration
Enrollment 150 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov