Status:
COMPLETED
Spine Patient Outcomes Registry for Biomet/EBI (Electro-Biology, Inc)
Lead Sponsor:
Zimmer Biomet
Conditions:
Degenerative Disc Disease
Spinal Stenosis
Eligibility:
All Genders
Brief Summary
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.
Detailed Description
A patient registry to prospectively collect data on patients who are having spinal surgery with EBI and Interpore Cross Spine Products.
Eligibility Criteria
Inclusion
- N/A
Exclusion
- N/A
Key Trial Info
Start Date :
April 1 2004
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
December 6 2007
Estimated Enrollment :
651 Patients enrolled
Trial Details
Trial ID
NCT00726284
Start Date
April 1 2004
End Date
December 6 2007
Last Update
February 24 2020
Active Locations (5)
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1
Neurological Surgery Associates
Little Rock, Arkansas, United States, 72205
2
Florida Orthopedics Association
Orange City, Florida, United States, 32763
3
CNS Healthcare
Akron, Ohio, United States, 44333
4
Oklahoma Spine and Brain
Tulsa, Oklahoma, United States, 74132