Registry study for familial cholesterol conditions
Part of Genetic & congenital, Hormones & metabolism clinical trials.
This trial is a global registry that collects health and genetic information from people with familial hypercholesterolemia (FH) and sometimes from their relatives. The goal is to better understand FH and how it presents, which can help improve care for families affected by high cholesterol.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You have a diagnosis of familial hypercholesterolemia (FH), either genetic or clinical, and it can be mild-to-severe (heterozygous or homozygous).
- Or you are a close relative of someone already diagnosed with FH and you were offered screening.
- Your information will be stripped of personal identifiers (de-identified) before it is shared for this registry.
- Your high cholesterol is not mainly caused by another treatable condition (for example, untreated thyroid problems, bile flow blockage, or kidney protein loss).
- Your local clinic must be able to collect and share your anonymized data according to local and country data standards.
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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This registry study collects information from people with familial hypercholesterolemia (a genetic condition causing very high cholesterol) to better understand the disease and improve care. By participating, you help researchers learn more about this condition.
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