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Clinical Trial Summary

Deep sedation in patients with COVID-19 may be challenging in many aspects. The use of an EEG-based protocol to guide deep sedation may be useful in this particular population, considering their unusually high sedation requirements. In the present trial, we aim to evaluate an EEG-based protocol to guide deep sedation in patients with COVID19, using to EEG derived parameters that are displayed in the BIS monitor: Suppression Rate and Spectral Edge Frequency. The protocol is designed to both minimize the suppression rate along with maintaining a spectral edge frequency over 10 Hz. The use of this protocol may reduce the amount of sedatives administered and, therefore, diminish the time needed for the weaning process.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04699916
Study type Interventional
Source University of Chile
Contact
Status Completed
Phase N/A
Start date January 4, 2021
Completion date September 23, 2021

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