Effect of Armolipid on Lipid Profile in Children With Hypercholesterolemia
Dyslipidemias, Children, Only
About this trial
This is an interventional treatment trial for Dyslipidemias
Eligibility Criteria
Inclusion Criteria: LDL-C >150 mg/dl in more than two measurements, after therapeutic lifestyle changes for at least 6 months. Exclusion Criteria: Secondary hypercholesterolemia Presence of any chronic disease or growth and developmental disorders Abnormal liver, kidney or thyroid function Prior use of hypolipidemic or other medication, at least 6 months before participation in the study.
Sites / Locations
- Lipid Outpatient Unit, 2nd Department of Pediatrics, Medical School, National and Kapodistrian University of Athens (NKUA), "P. & A. Kyriakou" Children's Hospital
Arms of the Study
Arm 1
Experimental
Armolipid
One tablet of Armolipid (Rottapharm S.p.A., Monza, Italia), containing 200 mg red yeast rice, 10 mg policosanols, 0.2 mg folic acid, 2.0 mg coenzyme Q10 and 0.5 mg astaxanthin was administered once-daily with lunch. Clinical and laboratory evaluation took place before and 6 (IQR: 5-8) and 16 (IQR: 11-19.7) months after treatment.