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Clinical Trial Summary

The purpose of this study was to compare the efficacy and safety of high dose atorvastatin (40 mg) versus high dose rosuvastatin (20 mg) in Egyptian type II diabetic patients with previous acute coronary syndrome history. This open-labeled prospective, randomized clinical trial compared once daily atorvastatin 40mg (Ator®) versus once daily rosuvastatin 20mg (Crestor®). The primary outcome was the 50% reduction in low-density lipoprotein cholesterol levels at 12 weeks. The secondary outcome was the achievement of low-density lipoprotein cholesterol level < 55 mg/dl.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05306990
Study type Interventional
Source Helwan University
Contact
Status Completed
Phase N/A
Start date April 20, 2017
Completion date January 31, 2021

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