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Intraoperative Monitoring (IOM) Patient Registry

NCT02187653 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 10000

Last updated 2014-07-11

No results posted yet for this study

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.

Conditions

  • Intraoperative Monitoring
  • Spinal Diseases

Sponsors & Collaborators

  • National Neurosurgical and Orthopedic Optimum Care Continuum (NOC2) Foundation

    collaborator UNKNOWN

  • National Research Independent Operations Management

    collaborator OTHER

  • DC2 Healthcare

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-09-30
Primary Completion
2016-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02187653 on ClinicalTrials.gov