Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
Completed
Conditions studied: Trauma, Tumor, Pseudarthrosis, Scoliosis, Degenerative Disc Disease
In brief
To prospectively collect radiographic and outcome data on patients who are having cervical spine fusion surgery with the VueLock™ Anterior Cervical Plate System
Key facts
- Study ID
- NCT00726128
- Run by
- Zimmer Biomet
- People needed
- 371
- Starts
- 1998-08-01
- Expected to finish
- 2009-09-01
- Last updated by the study team
- 2020-02-24
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- The patient will undergo anterior cervical fusion with the VueLock™ Anterior Cervical Plate System for treatment of degenerative disc disease (as defined by neck pain of discogenic origin of the disc confirmed by patient history and radiographic studies), trauma, tumors, deformity (defined as kyphosis, lordosis, or scoliosis), pseudarthrosis, and/or failed previous fusion.
- The patient must be available for follow-up during the study.
- The patient must be skeletally mature (epiphyses closed).
You may not qualify if…
- Patients with other pathology at the involved spinal level, e.g., osteomyelitis, Paget's disease, pathologic fracture, etc.
- Patients with a disease entity or condition that totally precludes the possibility of bony fusion such as known active cancer, etc.
- Pregnant or nursing females.
- Patients who in the opinion of the investigator would be psychologically unwilling or unable to understand or complete the protocol, especially those unwilling or unstable to participate in the follow-up.
Where it is running
- 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
Full record on ClinicalTrials.gov
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