Screening and Follow-up Study of Neonatal Jaundice Based on Mobile Network

  • STATUS
    Recruiting
  • End date
    Apr 30, 2025
  • participants needed
    4000
  • sponsor
    Nanjing Medical University
Updated on 19 February 2024
jaundice
hyperbilirubinemia
kernicterus

Summary

At least 13 hospitals in China will participate in the study, which aims to clarify the natural history of jaundice in Chinese healthy newbornsand decrease the incidence of severe hyperbilirubinemia and acute bilirubin encephalopathy and even kernicterus. The study is an open project, and the investigators welcome institutions fulfilling the specified requirements to join the study during the recruitment phase.

Description

This is a prospective cohort study of healthy term and near-term infants. The mobile network screening and follow-up of neonatal jaundice consists of two parts, one is the screening and follow-up program for healthy neonatal jaundice by using on parents' mobile phones, the other is the online registry of severe hyperbilirubinemia. Firstlythe TCB values of healthy term and near-term infants in delivery institutions will be prospectively recorded and followed up until jaundice subsided by using screening and follow-up program, so as to clarify the natural history of jaundice of healthy newborns in China. Secondly, by establishing an online registry for severe hyperbilirubinemia and "Follow up of jaundice" on Wechat applet, the investigators will find the specific problems of jaundice management in infants with severe hyperbilirubinemia. Lastly, through the follow-up of severe hyperbilirubinemia cases, the investigators will have a better understanding of their prognosis.

Details
Condition neonatal hyperbilirubinemia
Age 1years or below
Clinical Study IdentifierNCT04251286
SponsorNanjing Medical University
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Term or near-term neonates with gestational age 35w and birth weight 2000g

Exclusion Criteria

Biliary atresia, serious genetic and metabolic diseases, family history of epilepsy, and so on
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