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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Kuopio University Hospital

Kuopio, Northern Savonia, Finland, 70029

Comparison of the Nociception Monitoring Devices During Cardiac Surgery. | DecenTrialz