This study will evaluate and compare the effectiveness of MK-0653 (Vytorin) to current
standard treatment with other statins for the treatment of dyslipidemia in moderate,
moderately-high and high-risk participants.
Drug: Other Statin
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Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Pregnant or breastfeeding, or expecting to conceive within the projected duration of the study
Currently participating in or has previously participated in a study within 30 days
Congestive heart failure defined by New York Heart Association (NYHA) Class III or IV within previous 6 months
Uncontrolled cardiac arrhythmias or recent significant electrocardiogram (ECG) changes
Unstable angina pectoris
Myocardial infarction, coronary artery bypass surgery, or angioplasty within previous 3 months
Unstable or severe peripheral artery disease within previous 3 months
Uncontrolled hypertension (treated or untreated)
Type 1 or Type 2 diabetes mellitus that is poorly controlled or recently diagnosed
(within previous 3 months)
Uncontrolled endocrine or metabolic disease known to influence serum lipids or lipoproteins
Serious cerebrovascular disorder (ischemic stroke or cerebral hemorrhage) within the previous 6 months
Received treatment with systemic corticosteroids, any cyclical hormones within previous 8 weeks
All locations for NCT01587235
View full eligibility
Tris trial is registered with FDA with number: NCT01587235. The sponsor of the trial is Merck Sharp & Dohme Corp. and it is looking for 0 volunteers for the current phase.
Official trial title: A Multicenter, Open-label, 6 Week Study to Evaluate the Efficacy and Safety of Algorithm Based Intensive Treatment With Vytorin Versus Standard Treatment of Other Statins in Moderate, Moderately High and High Risk Patients.
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