Early Detection of Familial Hypercholesterolemia in Children

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age2-18
SponsorInstitut Investigacio Sanitaria Pere Virgili

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.

Eligibility criteria

Qualifiers

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).

Disqualifiers

The child population under 2 and over the age of 18 and children.

Children with high cholesterol but by secondary causes.

Trial design

Treatments tested in this trial

  • lifestyle assessment

Treatment groups

400 Participants
are divided into 2 treatment groups