Nutraceuticals to Improve Lipid Profile in European Countries (PIN)
Hyperlipidemia
About this trial
This is an interventional treatment trial for Hyperlipidemia focused on measuring Hyperlipidemia, Non-pharmacologic prevention
Eligibility Criteria
Inclusion Criteria:
- Class I indication to receive statin treatment but previous (<12 months) withdrawn of a statin due to side effects and unwilling to receive treatment with an alternative statin
- Class I indication to receive non-pharmacologic intervention and prevention strategies because of hyperlipidemia with 'low risk' classification
- Able to understand and willing to sign the informed CF
Exclusion Criteria:
• Women of child bearing potential patients must demonstrate a negative pregnancy test performed within 24 hours before CT
Sites / Locations
- Sapienza University
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Non-pharmacologic intervention
Nutraceuticals
Patients assigned by their own general practitioner to have non-pharmacologic intervention and prevention strategies will be given details on lifestyle approaches and dietary strategies
Patients assigned by their own general practitioner to receive nutraceuticals, along with non-pharmacologic intervention and prevention strategies, will have for 1 year also 1 capsule/day containing red yeast rice 200 mg, policosanol 10 mg, and berberine 500 mg,