The purpose of this study is to determine whether a loading dose of atorvastatin before
percutaneous intervention procedures in acute coronary syndromes is effective to reduce major
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Locations near you
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Full eligibility criteria for NCT01448642
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Acute coronary syndrome patients intending to undergo percutaneous coronary intervention.
Younger than 18 years
Presence of any contraindication to statin (Pregnant women, breast-feeding women or statin hypersensibility)
Advanced hepatic disease
Use of statins at the maximum dosage in the last 24 hours before the loading dose of the study drug
Use of fibrate in the last 24 hours
All locations for NCT01448642
Hospital do Coracao
Sao Paulo, SP, Brazil, 04005-000
View full eligibility
Tris trial is registered with FDA with number: NCT01448642. The sponsor of the trial is Hospital do Coracao and it is looking for 4191 volunteers for the current phase.
Official trial title: A Randomized, Multicenter Clinical Trial to Assess the Effect of Atorvastatin in Patients With Acute Coronary Syndrome and Intended Percutaneous Coronary Intervention
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