Clin2
NCT04370899Possibly a fitRecruiting

Early checkup for inherited high cholesterol in children

Familial HypercholesterolemiaFamilial Hypercholesterolemia - HeterozygousFamilial Hypercholesterolemia - Homozygous

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

This study looks at children who may have inherited high cholesterol, especially when one parent is affected. It may help doctors detect the condition earlier and understand how it runs in families.

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

Phase
N/A
Enrollment
400 people
Ages
2 years to 18 years
Study type
Observational

Who can take part

  • Your child is between 2 and 18 years old
  • Your child’s LDL (“bad cholesterol”) is above 135 mg/dL
  • A doctor has already ruled out common non-genetic causes of high cholesterol (like thyroid problems, kidney problems, diabetes, or certain kidney conditions)
  • One parent has a known genetic change (Lipoxip/Liponext) or a clinical diagnosis of familial high cholesterol
  • Your child does not have high cholesterol caused by a secondary (non-genetic) condition

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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