NCT04712773

Comparison of the Nociception Monitoring Devices During Cardiac Surgery.

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 40 (actual)
• Sponsor: Kuopio University Hospital · Academic / Other
• Sex: All
• Age: 18 Years – 75 Years
• Healthy volunteers: Not accepted

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 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.

Conditions

• Cardiac Surgery

Interventions

Type	Name	Description
DEVICE	PMD-200 monitor	Patient is connected to non-invasive PMD-200 monitor, measuring Nociception Level
DEVICE	Surgical Pleth Index monitor	Patient is connected to non-invasive monitor measuring Surgical Pleth Index

Timeline

• Start date: 2021-02-22
• Primary completion: 2025-03-01
• Completion: 2025-03-01
• First posted: 2021-01-15
• Last updated: 2025-03-06

Locations

1 site across 1 country: Finland