U.S., July 8 -- ClinicalTrials.gov registry received information related to the study (NCT07686341) titled 'PRecision Integrated Saturation Monitor' on June 30.
Brief Summary: 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.
Study Start Date: Aug., 2026
Study Type: OBSERVATIONAL
Condition:
CHD - Congenital Heart Disease
Singl...