Intraoperative Monitoring (IOM) Patient Registry

Status unconfirmed

Conditions studied: Intraoperative Monitoring, Spinal Diseases

In brief

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.

Key facts

Study ID

NCT02187653

Run by

DC2 Healthcare

People needed

10000

Starts

2011-09-01

Last updated by the study team

2014-07-11

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients undergoing lumbar or cervical surgery
• Utilization of IOM
• Understand and sign informed consent

You may not qualify if…

• There are no specific exclusion criteria

Where it is running

• DC2 Healthcare — Nashville, Tennessee, United States (enrolling)

Full record on ClinicalTrials.gov

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