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Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System

NCT00726128 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 371

Last updated 2020-02-24

No results posted yet for this study

Summary

To prospectively collect radiographic and outcome data on patients who are having cervical spine fusion surgery with the VueLock™ Anterior Cervical Plate System

Conditions

  • Trauma
  • Tumor
  • Pseudarthrosis
  • Scoliosis
  • Degenerative Disc Disease

Interventions

DEVICE

VueLock™ Anterior Cervical Plate

Implanted in subjects having an ACDF (Anterior cervical discectomy and fusion)

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • John Evangelsita, MD · EBI, LLC dba Biomet Spine, Biomet Trauma, Biomet Osteobiologics and Biomet Bracing

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
1998-08-31
Primary Completion
2009-09-30
Completion
2009-09-30

Countries

  • United States

Study Locations

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Entities

Diseases

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 NCT00726128 on ClinicalTrials.gov