Comparison of Onset of Neuromuscular Blockade With Electromyographic and Acceleromyographic Monitoring - Trial NCT05120999
Access comprehensive clinical trial information for NCT05120999 through Pure Global AI's free database. This phase not specified trial is sponsored by Mayo Clinic and is currently Completed. The study focuses on Neuromuscular Blockade. Target enrollment is 100 participants.
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Study Focus
Sponsor & Location
Mayo Clinic
Timeline & Enrollment
N/A
Oct 25, 2021
Jan 14, 2022
Primary Outcome
Time difference
Summary
The purpose of this research is to use 2 devices to compare the difference in the amount of
 time it takes for each device to register complete muscle relaxation after the muscle
 relaxing medication is given. The comparison will be made by using electromyographic (EMG),
 such as TetraGraph, and acceloromyographic (AMG), such as TOFScan, monitors at the time of
 insertion of breathing tube.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT05120999
Device Trial