Clinical Trials Directory

Trials / Completed

CompletedNCT06178848

EEG Parameters Between Remimazolam- and Propofol-based Anesthesia

Comparison of Quantitative EEG Parameters During Anesthesia Emergence Between Remimazolam Group and Propofol Group

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Yonsei University · Academic / Other
Sex
All
Age
19 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This is an observational study comparing perioperative quantitative EEG parameters between the conventional propofol/remifentanil and remimazolam/remifentanil. We aim to compare and analyze the differences in EEG patterns during the postoperative recovery in a group that underwent remimazolam and remifentanil-based total intravenous anesthesia(TIVA), in comparison to propofol and remifentanil-based TIVA

Conditions

Interventions

TypeNameDescription
DRUGpropofol groupDuring induction, the propofol group initiates with a target-controlled infusion (TCI) of propofol, starting at an effect site concentration of 4.0 ng/ml. After intubation, it is adjusted to maintain an appropriate depth of anesthesia based on the EEG (psi target 40).
DRUGremimazolam groupThe remimazolam group begins with a continuous infusion of remimazolam at 6 mg/kg/hr, which is then adjusted to 1 mg/kg/hr after loss of consciousness to maintain an appropriate depth of anesthesia based on the EEG (psi target 40).

Timeline

Start date
2023-06-26
Primary completion
2023-10-27
Completion
2023-10-27
First posted
2023-12-21
Last updated
2023-12-21

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT06178848. Inclusion in this directory is not an endorsement.