New study screens newborns for inherited high cholesterol
NCT ID NCT07470723
First seen Mar 14, 2026 · Last updated May 14, 2026 · Updated 9 times
Summary
This study aims to find different types of familial hypercholesterolemia (FH) in newborns. Parents will provide a cheek swab for genetic testing, and babies will have five blood samples collected over two years. The goal is to better understand and diagnose this inherited condition 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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