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Prospective Clinical Evaluation of the New Aegis Plate for Anterior Interbody Fusions

NCT00555659 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 104

Last updated 2013-08-12

No results posted yet for this study

Summary

Introduction: Degenerative changes of the discs and facet joints in the lumbar spine can result in pain and disability from spondylosis, spondylolisthesis and stenosis. Patients who are suffering with back and/or leg pain are potential candidates for an ALIF procedure.

Purpose: To assess and compare clinical outcomes and fusion rates in patients undergoing an instrumented ALIF procedure. Comparisons in all variables will be made across diagnostic categories. Comparisons between type of interbody spacer, graft type, and type of instrumentation will also be made

Conditions

  • Degeneration
  • Spondylosis
  • Spondylolithesis
  • Stenosis

Sponsors & Collaborators

  • DePuy Spine

    collaborator INDUSTRY

  • Columbia Orthopaedic Group, LLP

    lead OTHER

Principal Investigators

  • John D Miles, MD · Columbia Orthopaedic Group, LLP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-09-30
Primary Completion
2013-02-28
Completion
2013-02-28

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 NCT00555659 on ClinicalTrials.gov