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Comparison of the Nociception Monitoring Devices During Cardiac Surgery. — SYDNOS  

Cardiac Surgery Clinical Trial

Official title:
Comparison of the Nociception Monitoring Devices During Cardiac Surgery.

Clinical Trial Summary

The purpose of this study is to compare the values of Surgical Pleth Index (SPI) and Nociception Level Index (NOL) measured simultaneously during cardiac surgery.

Clinical Trial Description

Participants are given oral and written information about the course of the trial, associated risks and benefits and about the handling of the personal data on the day before the surgery by one of the investigators. Participants are also given written information about patient's rights and insurance, the aim of the trial and its course. 40 adult cardiac surgery patients will be recruited for the study. NOL and SPI values will be measured during the cardiac surgery procedure. All patients receive oral premedication and standardized anesthesia. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04712773
Study type Interventional
Source Kuopio University Hospital
Contact Pawel Florkiewicz, MD
Phone +358447175049
Email pawel.florkiewicz@kuh.fi
Status Recruiting
Phase N/A
Start date February 22, 2021
Completion date January 1, 2025
View Details
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