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Comparison of Onset of Neuromuscular Blockade With Electromyographic and Acceleromyographic Monitoring

NCT05120999 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2023-08-08

No results posted yet for this study

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.

Conditions

  • Neuromuscular Blockade

Interventions

DEVICE

Train of four measurement

Use of either TetraGraph or TOFScan to measure the neuromuscular blockade

Sponsors & Collaborators

Principal Investigators

  • J. Ross Renew, MD · Mayo Clinic

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-10-25
Primary Completion
2022-01-14
Completion
2022-01-14

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05120999 on ClinicalTrials.gov