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Posterior Cervical Fixation Study

NCT04770571 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2025-12-22

No results posted yet for this study

Summary

The objective of this study is to evaluate the safety and performance of occipito-cervico-thoracic spine surgery using posterior fixation as measured by reported complications, radiographic outcomes, and patients reported outcomes (PROs).This study is being undertaken to identify possible residual risks and to clarify mid-to long-term clinical performance that may affect the benefit/risk ratio of posterior fixation systems.

Conditions

  • Degenerative Disc Disease
  • Craniocervical Injuries
  • Cervical Radiculopathy
  • Cervical Disc Disease
  • Cervical Fusion
  • Cervical Spine Disease
  • Cervical Myelopathy
  • Cervical Instabilities Spine
  • Thoracic Injury

Interventions

DEVICE

observational study

observational

Sponsors & Collaborators

  • NuVasive

    lead INDUSTRY

Principal Investigators

  • Kyle Malone, MS · NuVasive

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-05-10
Primary Completion
2026-09-30
Completion
2028-11-30
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04770571 on ClinicalTrials.gov