Could genomic screening give every newborn a healthier start?
NCT ID NCT05990179
First seen Sep 30, 2025 · Last updated May 25, 2026 · Updated 34 times
Summary
This study explores whether advanced genomic sequencing can help screen newborns for rare genetic conditions beyond the standard tests. Researchers will invite families of 100,000 newborns to participate, offering optional screening for additional treatable or emerging conditions. The goal is to improve early detection and ensure all babies have an equal chance at a healthy life.
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the original study
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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.
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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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Columbia University Irving Medical Center/NYP
RECRUITINGNew York, New York, 10032, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact
Conditions
Explore the condition pages connected to this study.