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RecruitingAccepts healthy volunteers

NeuroVision vs Standard Neuromonitoring

Rush University Medical Center · NCT04639297

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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

NeuroVision vs Standard Neuromonitoring (NCT04639297) | Bored Studies