PRecision Integrated Saturation Monitor

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 information already being obtained while your baby is at the hospital.

NCT Number	NCT07686341
Lead Sponsor	Le Bonheur Children's Hospital Collaborators: The Consortium for Technology & Innovation in Pediatrics (CTIP)
Conditions	CHD - Congenital Heart Disease, Single Ventricle Heart Disease
Enrollment	100 participants
Start Date	2026-08
Primary Completion	2028-08 (estimated)
Study Completion	2028-12 (estimated)
Updated on ClinicalTrials.gov	2026-07-07