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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05521607
Other study ID # IRB22-0480
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 6, 2023
Est. completion date June 15, 2025

Study information

Verified date March 2024
Source Picterus AS
Contact Jeanmarie Schied, MD
Phone 7737029200
Email jschied@peds.bsd.uchicago.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A cross-sectional conductive study at the University of Chicago Medicine facilities (hospital and outreach clinics) to enable high qualitative estimation of bilirubin levels in the blood of newborns, independent of skin color, using Picterus JP.


Description:

A cross-sectional conductive study at the University of Chicago Medicine facilities (hospital and outreach clinics) will be conducted to include a total of 250 newborns with a desired distribution of skin color according to Neomar's scale : skin color 1 and 2: 20%, skin color 3: 30% and skin color 4: 50%. The Picterus Calibration Card will be placed on the chest of the newborn with the hole in the card placed over the infant's sternum. A validated smartphone with Picterus JP will be used to collect digital images..


Recruitment information / eligibility

Status Recruiting
Enrollment 250
Est. completion date June 15, 2025
Est. primary completion date June 15, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 1 Day to 14 Days
Eligibility Inclusion Criteria: - Infants born with gestational age > 37 weeks. - Birth weight = 2500 grams - Age 1 - 14 days - Infants requiring a TSB blood sample for clinically suspected jaundice as part of standard care Exclusion Criteria: - Infants showing signs of inborn disease. - Infants with skin rash or other skin disease that affects the skin where measurements are performed. - Infants transferred to the pediatric ward for medical treatment. - Infants that have received phototherapy in the last 24 hours

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Picterus Jaundice Pro (JP)
Use Picterus Jaundice Pro, a smartphone app that is used to take photo of the newborns skin, where the Picterus calibration card is place.

Locations

Country Name City State
United States University of Chicago Chicago Illinois

Sponsors (2)

Lead Sponsor Collaborator
Picterus AS University of Chicago

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Enable high qualitative estimation of bilirubin levels in the blood of newborns, independent of skin color, using Picterus JP. Evaluate of smartphone-based screening tool (Picterus JP) for neonatal jaundice in newborns with high melanin content. 3-6 months
Secondary Adapt the current algorithm of Picterus JP to newborns with high melanin content in the skin. Adapt the current algorithm of Picterus JP to newborns with high melanin content in the skin. 3-6months
Secondary Correlate estimates of bilirubin levels obtained by Picterus JP with TSB, TcB and VA in newborns with high melanin content in the skin. Correlate estimates of bilirubin levels obtained by Picterus JP with TSB, TcB and VA in newborns with high melanin content in the skin. 3-6 months
Secondary Determine the accuracy of Picterus JP in newborns with high melanin content in the skin. Determine the accuracy of Picterus JP in newborns with high melanin content in the skin. 3-6 months
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