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Study identifier: NCT07732244 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Evaluating a Wireless NIRS Device in the Neonatal Intensive Care Unit

Condition: Hypoxic-Ischemic Encephalopathy · Congenital Heart Disease · Stroke Hemorrhagic  ·  Sponsor: McGill University Health Centre/Research Institute of the McGill University Health Centre

PhaseNA
Planned participants20
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

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.).

This description comes directly from the study's public registry record.

Talk to the study team

Alyssa Maximov, BSc  ·  5149341934  ·  alyssa.maximov@muhc.mcgill.ca

Always discuss trial participation with your own doctor first.

Locations (1)

Montreal Children's HospitalMontreal, Quebec, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT07732244