The purpose of this patient registry is to prospectively collect data on patients who are having spinal surgery with EBI and Interpore Cross Spine Products.
A patient registry to prospectively collect data on patients who are having spinal surgery with EBI and Interpore Cross Spine Products.
Study Type
OBSERVATIONAL
Enrollment
651
Neurological Surgery Associates
Little Rock, Arkansas, United States
Florida Orthopedics Association
Orange City, Florida, United States
CNS Healthcare
Akron, Ohio, United States
Oklahoma Spine and Brain
Tulsa, Oklahoma, United States
Fusion Status
The primary outcome measure for this trial will be the percentage of successful fusions achieved.
Time frame: 24 Months
Mean VAS (Visual Analog Scale) Score Change from baseline
Time frame: 24 Month
Oswestry Disability Index / Neck Disability Index (which ever is appropriate for the subject) change from baseline
Time frame: 24 Month
neurologic Assessment - maintenance or Improvement
Time frame: 24 Month
SF-36 (Short Form Survey-36) Health Outcomes - Change from Baseline
Time frame: 24 Month
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Pottstown Memorial Medical Center
Pottstown, Pennsylvania, United States