Nutraceutical in Cardiovascular Primary Prevention (NIRVANA)
Hypercholesterolemia
About this trial
This is an interventional treatment trial for Hypercholesterolemia
Eligibility Criteria
Inclusion Criteria:
Age ≥18 years; Ability to provide informed written consent and to participate in the 16 weeks follow-up period And one of the following criteria
- Cardiovascular risk (SCORE) <1% and LDL levels ≥ 190 mg/dl (confirmed after a 4-week period of life style changes)
- Cardiovascular risk (SCORE) 1% to <5% and LDL levels ≥ 100 mg/dl (confirmed after a 4- week period of life style changes)
Exclusion Criteria:
Chronic liver disease Renal disease (creatinine clearance <60 mg/dl) Intolerance to nutraceutical compounds Thyroid disease Alcohol consumption >40 g/die Treatment with lipid lowering products in the previous 4 weeks Known coronary artery disease (CAD) or cerebrovascular disease Cardiovascular risk (SCORE) ≥5%
Sites / Locations
- University Hospital of Ferrara
Arms of the Study
Arm 1
Experimental
nutraceutical
after 4 weeks of lifestyle advice and changes, all subjects will receive for 8 weeks the administration of CARDIOVIS COLESTEROLO 3 mg, a nutraceutical compound containing containing red rice fermented with Monascus purpureus titrated with 3% monacolin K, hydrol mixture of olive fruit titrated with vitamin E, Coenzyme Q10 and polymethoxyflavones