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Comparison of the Nociception Monitoring Devices During Cardiac Surgery.

NCT04712773 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2025-03-06

No results posted yet for this study

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.

Conditions

  • Cardiac Surgery

Interventions

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

Sponsors & Collaborators

  • Kuopio University Hospital

    lead OTHER

Principal Investigators

  • Tadeusz Musialowicz, PhD, MD · Kuopio University Hospital, Department of Anesthesiology and Intensive Care

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-02-22
Primary Completion
2025-03-01
Completion
2025-03-01

Countries

  • Finland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04712773 on ClinicalTrials.gov