Family screening for familial high cholesterol
Part of Genetic & congenital, Hormones & metabolism clinical trials.
This trial is about helping families with familial hypercholesterolemia (a genetic condition that causes very high cholesterol) get screened. It tests a way to reach close relatives so they can learn their risk and consider next steps.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You are at least 18 years old
- You have a clinician-confirmed diagnosis of familial hypercholesterolemia
- You receive care through Penn Medicine
- You have contact info for at least one living parent, child, or full sibling (first-degree biological relative)
- You have a cell phone that can text and/or access to email
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 study uses a 'cascade testing' approach, where family members of people with familial hypercholesterolemia (FH), a genetic condition causing very high cholesterol, are tested to see if they also have it. The goal is to identify and test at-risk relatives early so they can get treatment to prevent heart problems.
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