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

Propofol Overdose of Undetermined Intent Clinical Trial

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

Status Completed

Clinical Trial Summary

The induction dose of propofol is generally determined based on patients' characteristics, underlying disease, general condition, and also by clinician's experiences. However, It is difficult to anticipate and objectively calculate an adequate dose of propofol for every patient considering the variability of an individual's response to propofol. If there is a specific pattern in EEG prior to induction of anesthesia that can provide information about the patient's susceptibility to propofol, every induction may be performed far more smoothly with a precisely optimized dose of propofol for each patient. The study is to find a relationship between the pre-induction EEG pattern of adult patients and their sensitivity to propofol.

Clinical Trial Description

n/a

Related Conditions & MeSH terms

• Drug Overdose
• Hypersensitivity
• Propofol Overdose of Undetermined Intent

• NCT number: NCT04520503
• Study type: Observational
• Source: Seoul National University Hospital
• Status: Completed
• Start date: September 9, 2020
• Completion date: February 28, 2022