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Clinical Trial Summary

Statin therapy does not fully eliminate the cardiovascular disease (CVD) risk associated with low high density lipoprotein-C (HDL-C) and high triglyceride levels. It is currently unknown what would be the best treatment option for patients with mixed hyperlipidemia who fail to meet their lipid targets with statin monotherapy at conventional does, i.e. high dose rosuvastatin or conventional statin dose plus micronized fenofibrate or conventional statin dose plus niacin/laropiprant. The aim of the present study is to compare the efficacy of high-dose rosuvastatin vs conventional statin dose plus micronized fenofibrate vs conventional statin dose plus extended-release niacin/laropiprant on lipid profile in patients with mixed hyperlipidemia. The primary efficacy endpoint will be changes in non-HDL-C levels at 6 months after treatment initiation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01010516
Study type Interventional
Source University of Ioannina
Contact Moses S Elisaf, MD
Phone +302651007509
Email egepi@cc.uoi.gr
Status Unknown status
Phase Phase 4
Start date October 2009

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