Median Nerve Electromyography to Monitor Intraoperative Neuromuscular Function

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorPongrácz Adrienn

About this trial

The effect of muscle relaxants need to be followed during surgery and before waking up the patient, the anesthesiologist has to make sure that the effect of muscle relaxants is gone. For this purpose, anesthesiologists use so called objective neurlmuscular monitors. These monitors stimulate the ulnar nerve in the wrist and examine the evoked muscle response. The aim of this study is to examine the usability of another nerve in the wrist, the median nerve.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

ASA I-III physical status

elective surgery requiring muscle relaxation

both arms are available during surgery in the same position for neuromuscular blockade monitoring

signed informed consent form

Disqualifiers

neruomuscular disorder in patient history (eg. stroke, myasthenia)

innervation problem in either arms (eg. carpal tunnel syndrome)

deformity to either arms (eg. Dupyurten contracture, severe arthritis)

Severe hepatic or renal insufficiency that affects muscle relaxant pharmacokinetics

Trial population

Adult patients undergoing elective surgery that requires one dose of non-depolarising neuromuscular blocking agent, whose arms are accessible for intraoperative neuromuscular blockade monitoring.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Electromyography

    Diagnostic test

    Electromyographic examination of the median and ulnar nerves to monitor intraoperative neuromuscular blockade

Treatment groups

45 Participants
are divided into 2 treatment groups
Group A: Median nerve examination1 intervention
Group B: Ulnar nerve examination1 intervention

Trial outcomes

Primary outcomes

1

CMAP

Comparison of compound muscle action potential amplitudes evoked by median and ulnar nerve stimulation and measured at the thenar

Time frame
Baseline

Secondary outcomes

1

Recovery time

Time from muscle relaxant administration to spontaneous recovery to TOFR\>0,9 monitored with median and ulnar nerve stimulation

Time frame
Perioperative
2

Onset time

Time from administration of muscle relaxant to disappearance of twitch response (TOFC0) monitored with median and ulnar nerve stimulation

Time frame
Baseline

Other outcomes

1

Bland-Altman analysis of TOFRs

Bland-Altman analysis of TOFRs obtained with medin and ulnar nerve stimulation

Time frame
Intraoperative
2

Bland-Altman analysis of TOFCs

Bland-Altman analysis of TOFCs obtained with median and ulnar nerve stimulation

Time frame
Intraoperative
3

Bland-Altman analysis of PTCs

Bland-Altman analysis of PTCs obtained with median and ulnar nerve stimulation

Time frame
Intraoperative
4

Baseline TOFRs

Examination of the stability of baseline TOFRs obtained with median and ulnar nerve stabilization

Time frame
Baseline

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Pongrácz Adrienn

Lead sponsor

University of Debrecen

Sponsor institution