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

C

Columbia Orthopaedic Group, LLP

Status

Completed

Conditions

Degeneration
Spondylolithesis
Spondylosis
Stenosis

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT00555659
1094241

Details and patient eligibility

About

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

Full description

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.

This study is part of a larger Continuous Quality Improvement initiative at the Columbia Orthopaedic Group. The purpose of this effort is to improve surgical and non-surgical outcomes by using rigorous statistical analysis of our outcomes to guide our treatment decisions. Through an iterative feedback process we hope to optimize patient outcomes.

Enrollment

104 patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Standard of care

Exclusion criteria

  • Standard of care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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