Ignite Creation Date:
2024-05-06 @ 3:07 PM
Last Modification Date:
2024-10-26 @ 1:43 PM
Study NCT ID:
NCT04520503
Status:
COMPLETED
Last Update Posted:
2023-10-16
First Post:
2020-08-05
Brief Title:
Relationship Between Pre-induction Electroencephalogram Pattern of Adult Patients and Their Sensitivity to Propofol
Sponsor:
Seoul National University Hospital
Organization:
Seoul National University Hospital
Study Overview
Official Title:
Relationship Between Pre-induction Electroencephalogram Pattern of Adult Patients and Their Sensitivity to Propofol
Status:
COMPLETED
Status Verified Date:
2023-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The induction dose of propofol is generally determined based on patients characteristics underlying disease general condition and also by clinicians experiences However It is difficult to anticipate and objectively calculate an adequate dose of propofol for every patient considering the variability of an individuals response to propofol If there is a specific pattern in EEG prior to induction of anesthesia that can provide information about the patients 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
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None