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Study identifier: NCT05632107 Synced from ClinicalTrials.gov · July 28, 2026
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Comparison of an Acceleromyography- and Electromyography-based Neuromuscular Monitor With TOF-Watch ® Monitor

Condition: Neuromuscular Blockade  ·  Sponsor: Huazhong University of Science and Technology

PhaseN/A
Planned participants100
Who can joinAll sexes, 18 Years to 90 Years
Healthy volunteersNo

About this study

A quantitative neuromuscular monitoring device is desirable to titrate the depth of neuromuscular block (NMB) during a procedure, and to prevent residual effects after removal of the endotracheal tube. Unfortunately, the most widely used monitoring technique acceleromyography (AMG) typically implies a series of cumbersome installation and calibration procedures that frequently precludes correct use of these devices in clinical practice. Electromyography (EMG) has recently attracted a lot of attention as an alternative strategy to compensate for the deficiency of AMG-based neuromuscular monitors. Nowadays, a new technology that allows for the simultaneous acquisition of EMG and AMG signals is commercially available. Although its reliability has been rapidly accepted in Physical Medicine and Rehabilitation, the use of the technique in neuromuscular monitoring has never been reported. The aim of the present study is to assess the validity of the new device for estimating the neuromuscular block by comparing with TOF Watch®-SX, which is the most widely accepted AMG-based neuromuscular monitor that has been practiced in the clinical arena for decades.

This description comes directly from the study's public registry record.

Talk to the study team

Hua Zheng, Dr.  ·  0086-27-83663173  ·  hzheng@hust.edu.cn

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Locations (2)

Department of Anaesthesiology, Tongji Hospital of Tongji Medical College, Huazhong University of Science and TechnologyWuhan, Hubei, ChinaRecruiting
Department of Anesthesiology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and TechnologyWuhan, Hubei, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT05632107