AI could revolutionize newborn screening for rare metabolic diseases
NCT ID NCT07368504
First seen Jan 28, 2026 · Last updated May 01, 2026 · Updated 11 times
Summary
This study will test whether an artificial intelligence (AI) system can accurately diagnose inherited metabolic disorders in newborns during routine screening. Researchers will compare the AI's results to standard manual interpretation by trained staff, using blood samples from 200,000 newborns. The goal is to see if the AI is more sensitive and specific, and if it reduces variability in screening results.
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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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The Children's Hospital, Zhejiang University School of Medicine
Hangzhou, Zhejiang, 310000, China
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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