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Intraoperative Monitoring (IOM) Patient Registry — IOM  

Spinal Diseases Clinical Trial

Official title:
Spine Registry Exposure for: Lumbar and Cervical Surgery Utilizing IOM

Clinical Trial 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 (motor and sensory) in the optimal management of the surgical patient.

Clinical Trial 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 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. ;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02187653
Study type Observational [Patient Registry]
Source DC2 Healthcare
Contact Christina R Cook, PhD
Phone 615-712-9574
Email ccook@dc2healthcare.com
Status Recruiting
Phase N/A
Start date September 2011
View Details
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