Effect of Ketamine Infusion on BIS Values

Status Completed

Clinical Trial Summary

Aim of this trial is to define if Concentration at the effector site (Ce) of Ketamine, during a continuous infusion and calculated with DOMINO model infusion pump are correlated with Bispectral Index BIS values during general anaesthesia for breast surgery.

Clinical Trial Description

Correlation between Concentration at the effector site (Ce) of Ketamine and Bispectral Index (BIS) values during general anaesthesia for breast surgery has not been defined yet during a continuous infusion. Authors want to analyze this correlation during general anaesthesia conducted using Propofol, ketamine and remifentanil. All of these drugs will be delivered with Target-Controlled Infusion pumps (in particular Eleveld for Propofol, Minto for Remifentanil and Domino for Ketamine). Ketamine will be observationally set at anaesthesiologist's discretion, but only CeK 0.1, 0.2, 0.4 and 0.6 for at least 30 minutes will be considered for analysis. ;

Study Design

Related Conditions & MeSH terms

Ketamine

Clinical Trial Details

NCT number	NCT05799729
Study type	Observational
Source	University of Padova
Contact
Status	Completed
Phase
Start date	April 1, 2023
Completion date	September 30, 2023

View Details

See also
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