Status:
UNKNOWN
Intraoperative Monitoring (IOM) Patient Registry
Lead Sponsor:
DC2 Healthcare
Collaborating Sponsors:
National Neurosurgical and Orthopedic Optimum Care Continuum (NOC2) Foundation
National Research Independent Operations Management
Conditions:
Intraoperative Monitoring
Spinal Diseases
Eligibility:
All Genders
18+ years
Brief Summary
The primary objective of this study is to evaluate the rate of new or worsening neurologic deficits and/or radiculopathy following lumbar or cervical surgery in light of IOM using neurological testing...
Detailed Description
Prospective reports will be collected on approximately 10,000 patients undergoing lumbar or cervical spinal surgery using intraoperative monitoring. Patients will be enrolled in registry after signing...
Eligibility Criteria
Inclusion
- Patients undergoing lumbar or cervical surgery
- Utilization of IOM
- Understand and sign informed consent
Exclusion
- There are no specific exclusion criteria
Key Trial Info
Start Date :
September 1 2011
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
Estimated Enrollment :
10000 Patients enrolled
Trial Details
Trial ID
NCT02187653
Start Date
September 1 2011
Last Update
July 11 2014
Active Locations (1)
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1
DC2 Healthcare
Nashville, Tennessee, United States, 37203