Early Detection of Familial Hypercholesterolemia in Children

Recruiting Observational Study
Familial Hypercholesterolemia Familial Hypercholesterolemia - Heterozygous Familial Hypercholesterolemia - Homozygous
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
2 – 18
Sex
Any
Study type
Observational
Participants needed
400 (estimated)
Sponsor
Institut Investigacio Sanitaria Pere Virgili · Other
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial

Heterozigous FH is an underdiagnosed disease in the paediatric population. Its early detection, would allow us to initiate lifestyle therapeutical changes and early pharmacological therapy if necessary. This is a key fact to reduce atherosclerosis progression and cardiovascular risk in adulthood. Moreover, it will allow, detecting the first and second degree affected relatives.

Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
Inclusion Criteria: * Children between 2 and 18 years of age. * LDL-C level above 135 mg/dL * Previously, the pediatrician will have discarded secondary causes (hypercholesterolaemia such as hypothyroidism, nephrotic syndrome, diabetes, renal insufficiency). After confirmation that one of the pare…
Contacts

Núria Plana, MD, PhD

+34977300310

nplana@grupsagessa.cat

CONTACT