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Intermountain Inpatient Bilirubin Decision Accuracy Study Using Smartphone-based Measurements by Picterus Jaundice Pro

Intermountain Inpatient Bilirubin Decision Accuracy Study Using Smartphone-based Measurements by Picterus Jaundice Pro

Recruiting
12-192 years
All
Phase N/A

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Overview

The goal of this project is to evaluate the performance of Picterus Jaundice Pro in an American population, including preterm and term newborns and pre- and post- phototherapy.

Description

The purpose of this study is to compare serum bilirubin levels with non-invasive bilirubin measurements in neonates during the first 12 to 192 hours of life using the "Picterus Jaundice Pro" smartphone application with a proprietary calibration card placed over the neonate's sternum. We will also validate the accuracy of Picterus Jaundice Pro bilirubin measurements before and after phototherapy treatment.

Eligibility

Inclusion Criteria:

  • the patient is free of skin rash, bruising, or other medical conditions that can interfere with transcutaneous measurement
  • (preterm) < = 35 weeks gestational age
  • (term) > 35 weeks gestational age
  • the patient has not been excluded by PI discretion.

Exclusion Criteria:

  • Neonates will be excluded from participation if all four inclusion criteria listed above are not met.

Study details
    Neonatal Jaundice

NCT06329843

Picterus AS

14 October 2025

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