PRecision Integrated Saturation Monitor
Recruiting
Observational Study
CHD - Congenital Heart Disease
Single Ventricle Heart Disease
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About This Trial
The purpose of this study is to find out if an abdominal pulse oximeter device is as accurate as a conventional fingertip pulse oximeter in pediatric patients. In this study, we will be collecting data from your medical record while you are being treated in the hospital for your clinical care. Your baby will be in the study for 3 days. There will be no additional study visits. We will collect info…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 0-12 months of age. (Must be less than 1 year of life for the pulse oximeter portion of the study) Weight greater than 2 Kg at time of study
* Admitted to an intensive care unit. (Not applicable for outpatient cohort)
* Arterial line in place as standard of care (Not applicabl…
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