NeuroVision vs Standard Neuromonitoring
Rush University Medical Center · NCT04639297
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Any age listed · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 148
- US sites recruiting
- 1
- Study start
- September 28, 2020
- Record last updated
- April 7, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The purpose of this study is to perform a prospective, randomized, controlled clinical trial to assess the utility of IONM in patients undergoing primary, single or multilevel lateral spinal procedures. Subjects will be randomized to undergo a lateral spine surgery with the use of NeuroVision® IONM or conventional hospital based IONM to assess incidence of new-onset neurological injury.
Being studied: NeuroVision® IONM; Hospital Based IONM
Conditions: Neurologic Deficits
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Patients undergoing a primary single or multilevel lateral spinal surgery procedures for degenerative pathology Diagnosis: myelopathy, radiculopathy, myeloradiculopathy, central stenosis, foraminal stenosis herniated nucleus pulposus, degenerative disc disease, spondylosis, and osteophytic complexes
- Patients able to provide informed consent
Exclusion Criteria
- Active infection
- Active or history of malignancy
- Spinal traumatic injury within the past 2 years
Recruiting US locations
Rush University Medical Center
Chicago, IL 60612
Site contact: Kern Singh, MD · 3124322888 · singh.research@rushortho.com
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