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Assessment of Neonatal Hyperbilirubinemia by NeoprediX B.1 Algorithm (Bili-PrediX1)

N

NeoPredix

Status

Completed

Conditions

Newborn Jaundice

Treatments

Diagnostic Test: NeoprediX B1 algorithm

Study type

Observational

Funder types

Industry
Other

Identifiers

NCT05121311
507/2021B02

Details and patient eligibility

About

Due to actual standard of neonatal care bilirubin is monitored in neonates several times after birth to avoid hyperbilirubinemia. As the peak is often one or two days after discharge from hospital a more precise predication than the actual one is desirable to avoid needlessly follow-ups. The precision of an algorithm to predict bilirubin values 24-48h into the future is evaluated in this study.

Full description

Neonatal jaundice is common and mostly transient without need for intervention. To identify infants at risk of bilirubin toxicity, bilirubin is measured several times after birth and before discharge home. As the peak bilirubin concentrations are reached at days 4-6 after birth, and most infants are discharged home around 48 hours after birth, parents are often asked to return to hospital one or two days after discharge with their newborn baby to have the bilirubin value checked in order to prevent that hyperbilirubinemia requiring treatment is not missed. A precise prediction of the course of bilirubin values based on the measurements done during the initial hospital stay after birth would be desirable to avoid unnecessary follow ups (both for the families and the health care system).

This study aims to evaluate the precision of the NeoprediX B1 algorithm. This algorithm predicts bilirubin values 24-48h into the future based on preceding values and some clinical variables. Five different scenarios will be explored, differing in the type, number and timepoints of measurements used for the prediction as well as the timepoint that is to be predicted.

Enrollment

455 patients

Sex

All

Ages

Under 72 hours old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Newborn infant
  • gestational age at birth ≥ 34+0/7 weeks

Exclusion criteria

  • Birth weight < 1500g
  • Gestational age at birth > 42+6/7 weeks
  • Genetically defined syndrome
  • Severe congenital malformation adversely affecting life expectancy or admission for a priori planned palliative care
  • Parents not fluent in German

Trial design

455 participants in 1 patient group

Newborns under bilirubin monitoring
Description:
Bilirubin monitoring according to standard of care of the participating center
Treatment:
Diagnostic Test: NeoprediX B1 algorithm

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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