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Atorvastatin in australia Patient population The study population was recruited as follows: Patients with primary or secondary coronary disease (CVD) were eligible for enrollment if the presence of apoB-100/SBP ratio greater than 3.55 was recorded in the clinical practice records or if there were sufficient clinical data available on the presence of arterial stiffness. A sample was recruited from the general hospital population and randomly allocated to receive either one tablet of amlodipine 50 mg for 10 days or placebo tablet twice daily for 10 days. All blood studies were approved by the institutional review board of University Minnesota. Patients were informed before administration of the study medication that they could stop the study medication at any time. As a study surrogate, we excluded all patients with any clinical or laboratory variables which were potentially associated with adverse effects (asthma, diabetes, liver, kidney, thyroid, and hypertension were excluded). We also excluded all patients diagnosed with a serious medical condition (e.g., heart, kidney, pancreatic) at baseline the University of Minnesota and excluded patients with a serum C-reactive protein level <4 mg/L or a serum LDL-cholesterol level <5.0 mmol/L due to ethical concerns. A total of 14,917 patients were enrolled between March 1, 2007, and June 30, 2008. Sample selection Patients were recruited from the general hospital population and randomly assigned to receive either one tablet of amlodipine 10 mg daily for days or placebo tablet four times daily for 10 days. Patients were also randomly assigned to receive either one tablet of fibrates 200 mg twice daily for 7 days or placebo tablet twice daily for 7 days, with a 10-day how much is atorvastatin in uk washout between the two groups each week for seven consecutive weeks. Exclusion criteria incl | ||