ISRCTN56034553已完成不适用
PREVEC Trial: Prevention of Reperfusion damage associated with percutaneous coronary angioplasty following acute myocardial infarction: a randomized double-blind placebo-controlled clinical trial
Scientific and Technological Development Fund (FONDECYT Fondo de Desarrollo Científico y Tecnológico) (Chile)0 个研究点目标入组 132 人开始时间: 2013年1月28日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 132
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Subjects may be of either sex and must be at least 18 years old
- •2. Subjects must have indication of primary percutaneous coronary angioplasty (PCA) as follows:
- •2.1. Angina or equivalent at least 120 min duration
- •2.2. Electrocardiogram (ECG) with STEMI that concerns more than 2 contiguous leads (>2mm)
- •3. Presentation within 12 h of symptoms onset
- •4. First myocardial infarction
- •5. Subject must be able and willing to sign informed consent
排除标准
- •1. History of renal or hepatic insufficiency
- •2. History of renal lithiasis (oxalates)
- •3. History of heart failure (NYHA III, IV)
- •4. Cardiogenic shock
- •5. Any serious medical co-morbidity that determine life expectancy < 6 month
- •6. Current participation in any other clinical investigation
- •7. Pregnancy
- •8. Glucose 6-phosphate dehydrogenase deficiency
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