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NCT07368504Likely a fitNot yet recruiting

Artificial intelligence for newborn metabolic screening

Inherited Metabolic Disorders

Part of Genetic & congenital clinical trials.

This study uses artificial intelligence (AI) to review newborn screening data for inherited metabolic diseases. It aims to improve early detection and help doctors identify at-risk babies sooner.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
200,000 people
Ages
2 days to 4 weeks
Study type
Interventional

Who can take part

  • Your baby had a routine newborn screening blood test for inherited metabolic disorders in the Zhejiang Provincial program between May 2025 and December 2027.
  • The blood sample was collected when your baby was between 2 and 28 days old.
  • Your baby's screening results and relevant health information are complete and available.
  • You don't have incomplete, poor-quality, or duplicate screening samples.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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