Intraoperative Monitoring (IOM) Patient Registry
| Status: | Recruiting |
|---|---|
| Conditions: | Orthopedic |
| Therapuetic Areas: | Orthopedics / Podiatry |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 4/2/2016 |
| Start Date: | September 2011 |
| Contact: | Christina R Cook, PhD |
| Email: | ccook@dc2healthcare.com |
| Phone: | 615-712-9574 |
Spine Registry Exposure for: Lumbar and Cervical Surgery Utilizing IOM
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 (motor and sensory) in the optimal management of the surgical patient.
deficits and/or radiculopathy following lumbar or cervical surgery in light of IOM using
neurological testing (motor and sensory) in the optimal management of the surgical patient.
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 informed consent. Data will be collected prior to surgery, during
surgery, immediately following surgery and 4 to 6 weeks post surgery. The registry will
serve as a database for surgeries using IOM.
Specific outcome measures will be: neurological assessment, length of hospital stay, pain
intensity, and complications.
cervical spinal surgery using intraoperative monitoring. Patients will be enrolled in
registry after signing informed consent. Data will be collected prior to surgery, during
surgery, immediately following surgery and 4 to 6 weeks post surgery. The registry will
serve as a database for surgeries using IOM.
Specific outcome measures will be: neurological assessment, length of hospital stay, pain
intensity, and complications.
Inclusion Criteria:
- Patients undergoing lumbar or cervical surgery
- Utilization of IOM
- Understand and sign informed consent
Exclusion Criteria:
- There are no specific exclusion criteria
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