Clin2
NCT06571630Likely a fitRecruiting

Familial high cholesterol registry

Familial Hypercholesterolemia

Part of Genetic & congenital, Hormones & metabolism clinical trials.

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.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
300 people
Ages
1 day and older
Study type
Observational

Who can take part

  • You have been diagnosed with familial hypercholesterolemia (a genetic condition that causes high cholesterol).

View the official record on ClinicalTrials.gov

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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