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

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 design

Treatments tested in this trial

  • Electromyography

Treatment groups

45 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Pongrácz Adrienn

Lead sponsor

University of Debrecen

Sponsor institution