Depth of Anesthesia Monitoring Clinical Trial
Official title:
BI-SENSES: Validation of Nasal Versus Frontal Placement of the SedLine® Sensor Through Processed Electroencephalography in Adult Patients Undergoing General Anesthesia
SedLine® Brain Function Monitoring provides real-time insight into a patient's depth of
anesthesia with bilateral data acquisition and processing of electroencephalogram (EEG)
signals. Four active EEG leads collect data from the frontal lobe with a sensor position on
the patient's forehead.
Whenever a frontal approach for neurosurgical procedures is required or the frontal placement
of the EEG is not indicated, it would not be possible to place the SedLine® .
Numerous studies have analyzed the change of position and the application of alternative
positions for other devices used in assessing the depth of anesthesia. Albeit, yet to date,
there is no study that analyzed the application of alternative positions for the SedLine®
sensor.
The purpose of study is to compare the standard forehead placement versus a nasal placement
of SedLine® sensor for neuromonitoring.
The hypothesis is that placing the central sensors in the montage approximately 2 cm below
the standard recommended placement, across the nasal bridge and then running under the eyes
to the normal temporal leads placement would put the entire montage out of the operative
field and would still have corresponding values and EEG signals.
The primary outcome measure is to monitor and compare processed electroencephalograph (EEG)
values (PSi- Patient State Index, SEFL- Spectral Edge Frequency Left, SEFR- Spectral Edge
Frequency Right, SR-Suppression Ratio, EMG-Electromyography, ARTF-Artifact) and EEG
waveforms, on both sensors (standard-Forehead and alternative-Nasal)
Other parameters that will be measure are patient demographics (age, sex, surgery, ASA
status, weight, height, BMI).
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