Spine Patient Outcomes Registry for Biomet/EBI (Electro-Biology, Inc)
Completed
Conditions studied: Degenerative Disc Disease, Spinal Stenosis
In brief
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.
Key facts
- Study ID
- NCT00726284
- Run by
- Zimmer Biomet
- People needed
- 651
- Starts
- 2004-04-01
- Expected to finish
- 2007-12-06
- Last updated by the study team
- 2020-02-24
Who can join
Age: any. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- N/A
You may not qualify if…
- N/A
Where it is running
- 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
- Pottstown Memorial Medical Center — Pottstown, Pennsylvania, United States
Full record on ClinicalTrials.gov
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