CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 78 enrolled
Drug / intervention
Standardized Propofol Administrationdrug
Likely dose
Standardized Propofol Administration 0.5 mg/Kgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04713644
NCT04713644N/ACompleted

Study of the Association Between Burst Suppression During Anesthetic Induction With Propofol in Cardiac Surgery in Patients Over 65 Years of Age With Postoperative Delirium

Pontificia Universidad Catolica de Chile·observational·Posted Jan 19, 2021·Updated May 31, 2025

In Brief

An observational study evaluating Standardized Propofol Administration for Postoperative Delirium. Completed, enrolled 78 participants across 1 site.

Detailed Summary

The population over 65 years of age will be increasingly exposed to surgical procedures that require general anesthesia. Postoperative delirium is one of the main causes of preventable postoperative morbidity in the elderly population and is a frequent event after cardiac surgery with extracorporeal circulation. The excess administration of anesthetics that potentiate the Gamma Aminobutyric A receptor, such as propofol, are related to an intraoperative electroencephalographic pattern called burst suppression that has been associated with postoperative delirium. It is unknown whether this pattern is secondary to a relative overdose of anesthetics or rather corresponds to a characteristic of a vulnerable brain that is suppressed at doses at which other patients are not. Our objective will be to determine whether burst suppression in people over 65 years of age during a standardized anesthetic induction with propofol for cardiac surgery with extracorporeal circulation is associated with postoperative delirium compared to older people who do not present it.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesChile
Collaborators--

Timeline

N/ACompletedFinished
202120222023202420252026
First PostedJan 19, 2021
Enrollment StartMar 1, 2021
Primary CompletionFeb 28, 2024
Study CompletionSep 1, 2024
TodayJul 2, 2026
Enrollment to primary: 3.0 yearsPosted 5.5 years ago

Interventions

Standardized Propofol Administrationdrug

Intravenous bolus propofol administration of 0.5 mg/Kg dose, plus 0.5 mg/Kg extra if necessary