Perfusion Index Parameter

Completed

Conditions studied: Perfusion; Complications

In brief

To evaluate the association between the Perfusion index parameter and an independent measure of perfusion.

Key facts

Study ID

NCT06586918

Run by

Medtronic - MITG

People needed

32

Starts

2024-09-04

Expected to finish

2024-09-13

Last updated by the study team

2026-05-15

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Subjects ≥18 years of age
• Subject is able to participate for the duration of the study
• Subject is willing to sign an informed consent
• Subject weighs >40kg

You may not qualify if…

• Previous injury or trauma to fingers or hands that may change blood flow or vascular supply and affect the ability to test sensors
• Physiologic abnormalities that prevent proper application of pulse oximetry sensor
• Severe contact allergies that cause a reaction to standard adhesive materials such as those found in medical sensors and electrodes.
• Raynaud Syndrome
• Repeated systolic blood pressure > 140mmHg -

Where it is running

• Medtronic Clinical Physiology Lab — Denver, Colorado, United States

Full record on ClinicalTrials.gov

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