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Comparing Skin Conductance and Nol-index

Anesthesia Clinical Trial

Official title:
Nociceptive Monitoring With Skin Conductance and Nol-index in Moderate-to-high Risk Cardiovascular Patients

Clinical Trial Summary

Comparison of twà different nociception monitors during general anesthesia

Clinical Trial Description

Analgesia remains a challenge in anesthesia. Several monitors have shown potential in detecting insufficient analgesia during general anesthesia, but they have not been investigated in patients undergoing cardiac and vascular surgery. In this study, we will compare skin conductance (Medstorm, Norway) and nol-index (Medasense, Israel) w during noxious and non-noxious stimuli. This study is carried out on patients included in another study (Nol-Index Guided Remifentanil Analgesia Versus Standard Analgesia During Moderate-to-High Risk Cardiovascular Surgery). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04138966
Study type Observational
Source Erasme University Hospital
Contact Sean Coeckelenbergh, MD
Phone 32 (0) 2 555 39 19
Email secoecke@ulb.ac.be
Status Recruiting
Phase
Start date October 20, 2019
Completion date December 20, 2020
View Details
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