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Study identifier: NCT04639297 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

NeuroVision vs Standard Neuromonitoring

Condition: Neurologic Deficits  ·  Sponsor: Rush University Medical Center

PhaseNA
Planned participants148
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersYes

About this study

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.

This description comes directly from the study's public registry record.

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Contact details are listed per location below or on the registry record.

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Locations (1)

Rush University Medical CenterChicago, Illinois, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT04639297