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Clinical Trials/NCT04471376
NCT04471376
Completed
Not Applicable

Intraoperative Reversal of Muscle Relaxants During Transcranial Electrical Motor Evoked Potential Monitoring in Patients Undergoing Spinal Surgery

Beijing Tiantan Hospital1 site in 1 country66 target enrollmentJuly 16, 2020
ConditionsSugammadex
InterventionsSugammadex

Overview

Phase
Not Applicable
Intervention
Sugammadex
Conditions
Sugammadex
Sponsor
Beijing Tiantan Hospital
Enrollment
66
Locations
1
Primary Endpoint
The amplitude of MEP
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Transcranial motor evoked potential (TcMEP) monitoring is conventionally performed during neurosurgical procedures without or with minimal neuromuscular blockade (NMB) because of its potential interference with signal interpretation. However, full blockade offers increased anesthetic management options and facilitates surgery. Here, investigators want to assess the effect of Sugammadex during TcMEP in adult patients. Sugammadex is designed to encapsulate rocuronium and reverse rocuronium-induced neuromuscular blockade. 64 patients undergoing thoracic or lumbar spinal surgery will be randomly allocated into sugammadex group or control group under a ratio of 1 to 1. Patients will receive either continuous infusion of rocuronium to produce blockade maintained at least two twitches in Train-of-Four (TOF), rocuronium infusion will be discontinued and 2 mg/kg of sugammadex will be infused while dura opening in sugammadex group. Whereas no muscle relaxant will be given after anesthetic induction in control group. The primary aim of this study is to compare mean value of amplitudes of TcMEPs in abductor pollicis brevis muscles of both upper extremities 5 minutes after dura opening.

Registry
clinicaltrials.gov
Start Date
July 16, 2020
End Date
December 31, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Beijing Tiantan Hospital
Responsible Party
Principal Investigator
Principal Investigator

Ruquan Han

Principal Investigator

Beijing Tiantan Hospital

Eligibility Criteria

Inclusion Criteria

  • 18-65 years
  • ASA status I-II
  • Patients undergo thoracic or lumbar spinal surgery
  • tcMEP monitoring during the surgery
  • Informed consent signed by patients

Exclusion Criteria

  • BMI ≥35 Kg/m-2
  • history of epilepsy or use of antiepileptic drugs, neuromuscular disorder(s)
  • history or family history of malignant hyperthermia
  • allergies to sugammadex, NMBs or other medication(s) used during general anesthesia
  • anemia, hemoglobin \<110g/L,
  • TcMEPs stimulate or record site infection
  • preoperative neurological dysfunction in both upper extremities
  • cardiac pacemaker
  • pregnancy and breast-feeding

Arms & Interventions

Sugammadex group

Intervention: Sugammadex

Outcomes

Primary Outcomes

The amplitude of MEP

Time Frame: 5 minutes after dura opening

mean value of amplitudes of TceMEPs in abductor pollicis brevis muscles of both upper extremities

Secondary Outcomes

  • The latencies of MEPs(5, 10, 20, 30 and 60 minutes after dura opening.)
  • Respiratory parameters(during the surgery)
  • Adverse effects of sugammadex(during and 24 hours after the surgery)
  • Incidence of body movement(during the surgery)
  • The amplitude of MEP(10, 20, 30 and 60 minutes after dura opening)
  • Motor function assessment(5 days after surgery)
  • Total bleeding volume(during the surgery)
  • Recurrence of neuromuscular blockade(At the end of surgery)

Study Sites (1)

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