New registry aims to track rare cholesterol disease in children and adults
NCT ID NCT01109368
First seen May 08, 2026 · Last updated May 10, 2026 · Updated 1 time
Summary
This study creates a registry to monitor the health and artery cholesterol levels of children and adults with homozygous familial hypercholesterolemia (hoFH), a rare genetic condition causing extremely high cholesterol from birth. Researchers will collect medical data and blood samples to understand how the disease progresses and how different treatments affect it. The goal is to improve future care and develop better therapies for this serious condition.
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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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Phone: •••-•••-•••• Email: •••••@•••••
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Weill Cornell Medical College
RECRUITINGNew York, New York, 10021, United States
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