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UnknownNCT04138966

Comparing Skin Conductance and Nol-index

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

Status
Unknown
Phase
Study type
Observational
Enrollment
10 (estimated)
Sponsor
Erasme University Hospital · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers

Summary

Comparison of twà different nociception monitors during general anesthesia

Detailed 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).

Conditions

Interventions

TypeNameDescription
DEVICENol-IndexMultiparametric monitor that studies that establishes an index as a surrogate to nociception
DEVICESkin ConductanceMeasures skin conductance as a surrogate to nociception

Timeline

Start date
2019-10-20
Primary completion
2020-06-01
Completion
2020-12-20
First posted
2019-10-25
Last updated
2020-11-09

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT04138966. Inclusion in this directory is not an endorsement.

Comparing Skin Conductance and Nol-index (NCT04138966) · Clinical Trials Directory