A unicenter, randomized, double-blind, parallel-group, placebo-controlled study of Melatonin as an Adjunct in patients with acute myocaRdial Infarction undergoing primary Angioplasty - The Melatonin Adjunct in the acute myocaRdial Infarction treated with Angioplasty (MARIA) trial: Study design and rationale

被引:59
作者
Dominguez-Rodriguez, Alberto
Abreu-Gonzalez, Pedro
Garcia-Gonzalez, Martin J.
Kaski, Juan Carlos
Reiter, Russel J.
Jimenez-Sosa, Alejandro
机构
[1] Univ Hosp Canarias, Dept Cardiol, Coronary Care Unit, E-38320 Tenerife, Spain
[2] Univ La Laguna, Sch Med, Dept Physiol, Tenerife, Spain
[3] St Georges Univ London, Cardiovasc Biol Res Ctr, Div Cardiac & Vasc Sci, London, England
[4] Univ Texas, Hlth Sci Ctr, Dept Cellular & Struct Biol, San Antonio, TX 78284 USA
[5] Univ Hosp Canarias, Res Unit, E-38320 Tenerife, Spain
关键词
melatonin; acute myocardial infarction; primary angioplasty; study design; phase; 2;
D O I
10.1016/j.cct.2006.10.007
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Experimental studies have documented the beneficial effects of the endogenously produced antioxidant, melatonin, in reducing tissue damage and limiting cardiac pathophysiology in models of experimental ischemia-reperfusion. Melatonin confers cardioprotection against ischemia-reperfusion injury most likely through its direct free radical scavenging activities and its indirect actions in stimulating antioxidant enzymes. These actions of melatonin permit it to reduce molecular damage and limit infarct size in experimental models of transient ischemia and subsequent reperfusion. Study design: The Melatonin Adjunct in the acute myocaRdial Infarction treated with Angioplasty (MARIA) trial is an unicenter, prospective, randomized, double-blind, placebo-controlled, phase 2 study of the intravenous administration of melatonin. The primary efficacy end point of this study is to determine whether melatonin treatment reduces infarct size determined by the cumulative release of alpha-hydroxybutyrate dehydrogenase (area under the curve: 0 to 72 h). Other secondary end points will be the clinical events occurring within the first 90 days: death, sustained ventricular arrhythmias, resuscitation from cardiac arrest, cardiogenic shock, heart failure, major bleedings, stroke, need for revascularization, recurrent ischemia, re-infarctions and rehospitalization. Implications: The MARIA trial tests a novel pharmacologic agent, melatonin, in patients with acute myocardial infarction and the hypothesis that it will confer cardioprotection against ischemia-reperfusion injury. If successful, the finding would support the use of melatonin in therapy of ischemic-reperfusion injury of the heart. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:532 / 539
页数:8
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