Spots Global Cancer Trial Database for Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
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Trial Identification
Brief Title: Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
Official Title: A Multi-Center Prospective Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
Study ID: NCT00726128
Interventions
Study Description
Brief Summary: To prospectively collect radiographic and outcome data on patients who are having cervical spine fusion surgery with the VueLock™ Anterior Cervical Plate System
Detailed Description: The purpose is to prospectively collect radiographic and outcome data on patients who are having cervical spine fusion surgery with the VueLock™ Anterior Cervical Plate System.
Keywords
Eligibility
Minimum Age:
Eligible Ages: CHILD, ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Locations
Palo Alto Medical Foundation, Palo Alto, California, United States
Alvarado Orthopedic Clinic, San Diego, California, United States
American health Network, Avon, Indiana, United States
Raliegh Orthopedic Research Foundation, Raleigh, North Carolina, United States
Contact Details
Name: John Evangelsita, MD
Affiliation: EBI, LLC dba Biomet Spine, Biomet Trauma, Biomet Osteobiologics and Biomet Bracing
Role: STUDY_CHAIR
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