NCT04520503View on ClinicalTrials.gov

Relationship Between Pre-induction Electroencephalogram Pattern of Adult Patients and Their Sensitivity to Propofol

CompletedOBSERVATIONAL
Enrollment

70

Participants

Timeline

Start Date

September 9, 2020

Primary Completion Date

February 28, 2022

Study Completion Date

February 28, 2022

Conditions
Propofol Overdose of Undetermined Intent
Interventions
DRUG

Propofol

The dose of propofol required for loss of consciousness and the total induction dose of propofol will be recorded for every patients.

DEVICE

EEG monitoring

The processed EEG spectrogram and indices, such as patient status index, 95% spectral edge frequency, and suppression ratio, will be obtained from Sedline monitoring device. The raw pre-induction EEG will be extracted from Sedline at the end of induction and it will be analyzed by an external software to calculate the mean frequency, frequency band power and its distribution.

Trial Locations (1)

03080

Seoul National University Hospital, Seoul

All Listed Sponsors
lead

Seoul National University Hospital

OTHER

NCT04520503 - Relationship Between Pre-induction Electroencephalogram Pattern of Adult Patients and Their Sensitivity to Propofol | Biotech Hunter | Biotech Hunter