RecruitingNot ApplicableNCT07732244

Evaluating a Wireless NIRS Device in the Neonatal Intensive Care Unit

Evaluating a Wireless NIRS Device in the Neonatal Intensive Care Unit: a Sub-study of the Wireless NICU Study


Sponsor

McGill University Health Centre/Research Institute of the McGill University Health Centre

Enrollment

20 participants

Start Date

Nov 15, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The wireless NIRS sensor will be placed on the participant's forehead, directly underneath the INVOS wired sensor. The wireless NIRS sensor will remain in place for 4 consecutive hours, over 2 consecutive days. As standard-of-care, nursing personnel removes all sensors at every care to evaluate skin and reduce the risk of pressure sores. The wireless NIRS device will be removed and reapplied at the same time, by the research team who will annotate what time the sensor was removed, replaced, and the condition of the skin. This will be used to correlate signal disconnection with sensor care (i.e., skin checks, sensor removal, etc.).


Eligibility

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called Wireless NIRS for people with aneurysm cerebral, congenital heart disease, and other related conditions. The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEWireless NIRS

Wireless NIRS applied to participant forehead.


Locations(1)

Montreal Children's Hospital

Montreal, Quebec, Canada

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NCT07732244


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