ConditionsFamilial HypercholesterolemiaFamilial Hypercholesterolemia - HeterozygousFamilial Hypercholesterolemia - Homozygous
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 groupsSponsors and collaborators
Source ClinicalTrials.gov