Clin2
NCT04529967Likely a fitRecruiting

Screening kids for inherited high cholesterol

Familial Hypercholesterolemia

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

This study checks children ages 1 to 3 during routine care to see who may have familial hypercholesterolemia, a genetic condition that causes high cholesterol. Early identification can help families learn about next steps and prevention.

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

Phase
N/A
Enrollment
15,000 people
Ages
1 year to 3 years
Study type
Observational

Who can take part

  • Your child is able to come for screening as part of routine child care
  • Your child is between 1 and 3 years old at the time of the study visit

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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