A Study Of Remifentanil Vs Neuromuscular Blockade For Intubation During Spine Surgery With MEP Monitoring

Overview

About this study

The purpose of this study is to compare intubating conditions among four anesthesia induction strategies: remifentanil 2 mcg/kg, remifentanil 4 mcg/kg, succinylcholine, and rocuronium/sugammadex in patients undergoing spine surgery requiring motor evoked potential monitoring.

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:

  • Adults aged 18-75 years

  • American Society of Anesthesiologists (ASA) physical status I-III

  • Scheduled for elective spine surgery (cervical, thoracic, or lumbar) requiring intraoperative MEP monitoring

  • Able to provide written informed consent

Exclusion Criteria:

  • Known or suspected difficult airway (Mallampati class IV, history of difficult intubation, limited mouth opening < 3 cm, limited neck extension)

  • Body mass index (BMI) > 40 kg/m2

  • Known allergy or hypersensitivity to remifentanil, succinylcholine, rocuronium, sugammadex, or propofol

  • Personal or family history of malignant hyperthermia • Known or suspected pseudocholinesterase deficiency

  • Conditions predisposing to succinylcholine-induced hyperkalemia (e.g., major burns within the last year, denervation injuries or upper motor neuron lesions within 6 months, severe crush injuries, prolonged immobilization > 72 hours, known hyperkalemia > 5.5 mEq/L)

  • Severe preoperative motor deficit (manual muscle testing ≤ 2/5 in monitored extremities)

  • Neuromuscular disorders (e.g., myasthenia gravis, muscular dystrophy, Guillain-Barre syndrome, prior stroke with residual motor deficits)

  • Severe cardiovascular disease (e.g., ejection fraction < 30%, unstable angina, myocardial infarction within 3 months)

  • Severe bradycardia (heart rate < 50 bpm) or high-grade atrioventricular block without a pacemaker

  • Current use of medications affecting neuromuscular function (aminoglycosides, magnesium infusion, certain antiepileptic meds, etc.)

  • Emergency surgery

  • High aspiration risk (e.g., uncontrolled gastroesophageal reflux disease)

  • Pregnancy or breastfeeding

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

Eligibility last updated 06/28/2026. 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

Jacksonville, Fla.

Mayo Clinic principal investigator

Shaun Gruenbaum, M.D., Ph.D.

Open for enrollment

Contact information:

Shaun Gruenbaum

9049563004

gruenbaum.shaun@mayo.edu

More information

Publications

Publications are currently not available