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Long-term Assessment of the Safety and Performance of the NuVasive Simplify Disc

StatusActive, Not Recruiting
PhaseNot specified
SponsorNuVasive
Started
View on ClinicalTrials.gov ↗

Record History

  1. Re-verified, no change to tracked fieldsv6
  2. Trial status: Enrolling by Invitation to Active, Not Recruitingv5
  3. Study sites: 9 to 10v4
  4. Study sites: 6 to 9v3
  5. Study sites: 3 to 6
    • Start date changed from estimate of Feb 2022 to Feb 9, 2022
    • Secondary endpoints: details revised at 8 of 12 entries
    v2
  6. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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
See all monitored trials
A prospective, multicenter post-market clinical follow-up study to evaluate the 10-year long-term safety and effectiveness of the Simplify Disc in subjects who were enrolled in the post approval study (NCT04630626).
Trial Details
NCT Number NCT05258435
Lead Sponsor NuVasive
Conditions
(from sponsor)		 Cervical Disc Disease, Degenerative Disc Disease
Related terms Intervertebral Disc Degeneration
Enrollment 131 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov