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Clinical Trial Summary

Verification of biomarkers in a human population for their ability to diagnose the severity of neonatal asphyxia. These biomarkers linked to asphyxia have been identified in animal studies.


Clinical Trial Description

The aim of the study is to verify the application of combinations of several laboratory parameters in early postnatal blood samples, for identification of infants, who will suffer from early abnormal neonatal neurological outcome, in a population at risk. The population at risk is defined as term and late preterm (>36 weeks of gestation) human infants following perinatal hypoxia-ischemia with or without postnatal resuscitation. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03354208
Study type Observational [Patient Registry]
Source Life Science Inkubator
Contact
Status Completed
Phase
Start date October 2016
Completion date December 27, 2017

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