A Study Of Multi-channel Accelerometry During Intraoperative Neuromonitoring

Overview

About this study

The purpose of this study is to determine if supramaximal LQP stimulation has: (a) superior tcMEP signal size and reliability; (b) less truncal and limb body movement; (c) reduced current and charge requirements, when compared against bipolar stimulation.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:  

  • 18 or older with full capacity to make decisions

  • Undergoing non-emergent cervical, thoracic, or lumbar spine surgery

  • No compressive myelomalacia on MR imaging

  • No history of limb amputation

Exclusion Criteria: 

  • [Baseline neurologic exam] Preoperative exam worse than -1 strength on Mayo rating scale (or worse than 4+/5 on the Medical research council strength scale) for the monitored muscles

  • [Determined in OR, anesthesia compatibility] Anesthesia need for use of dexmedetomidine, inhalational anesthetics, or neuromuscular blockade at time of baseline signal acquisition (a short course of these drugs at time of intubation is acceptable)

  • [determined in OR: MEP reliability] Upon best optimization with either bipolar or LQP, tcMEP response from at least one muscle among left and right abductor digiti minimi, tibialis anterior, or abductor hallucis, at time of baseline is any of the following:

    • < 1000 μV*ms area under the curve

    • Qualitatively high trial-to-trial variability on visual inspection

    • Absent or only inconsistently present

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 04/06/2026. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Tatsuya Oishi, M.D.

Open for enrollment

Contact information:

Tatsuya Oishi

oishi.tatsuya@mayo.edu

More information

Publications

Publications are currently not available
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CLS-20599212

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