New study screens newborns for inherited high cholesterol
NCT ID NCT07470723
First seen Mar 14, 2026 · Last updated May 01, 2026 · Updated 6 times
Summary
This study aims to identify familial hypercholesterolemia (FH), a genetic condition causing high cholesterol, in newborns. Researchers will collect cheek swabs from parents and blood samples from babies over 2 years. The goal is to better understand how to detect FH early in life.
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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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Study contacts
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Contact
Email: •••••@•••••
Locations
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University of Wisconsin - Madison
RECRUITINGMadison, Wisconsin, 53792, United States
Contact Email: •••••@•••••
Conditions
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