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Clinical Trial Summary

The purpose of this study is early identification of asphyxiated newborns through eeg starting in the delivery room.


Clinical Trial Description

There is a need for a reliable detector of birth asphyxia so that newborns with birth asphyxia can have timely and accurate diagnosis to receive therapeutic hypothermia within 6 hrs of life, which has been shown to significantly reduce deaths and improve long term developmental outcomes.

This study is designed to record EEG during birth transition through the first 10 minutes of life. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02445417
Study type Observational
Source Sharp HealthCare
Contact
Status Completed
Phase
Start date June 25, 2015

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