Status:
COMPLETED
Comparison of the Nociception Monitoring Devices During Cardiac Surgery.
Lead Sponsor:
Kuopio University Hospital
Conditions:
Cardiac Surgery
Eligibility:
All Genders
18-75 years
Phase:
NA
Brief 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.
Detailed 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...
Eligibility Criteria
Inclusion
- coronary artery disease of heart valve disorder qualified for the surgical treatment
- participant understands the course of the trial and its aim
- participant has given informed written consent
Exclusion
- participant has not given consent
- neurological or psychical disorders (psychiatric medication)
- dementia
- alcohol or substance abuse
- central nervous system medication (medication for epilepsy or neuropathic pain)
Key Trial Info
Start Date :
February 22 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2025
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT04712773
Start Date
February 22 2021
End Date
March 1 2025
Last Update
March 6 2025
Active Locations (1)
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1
Kuopio University Hospital
Kuopio, Northern Savonia, Finland, 70029