跳至主要内容
临床试验/NCT00610870
NCT00610870已完成不适用

Effect of Atorvastatin Administration Before Primary Percutaneous Coronary Intervention in Patients With ST-segment Elevation Myocardial Infarction

Samsung Medical Center1 个研究点 分布在 1 个国家目标入组 173 人开始时间: 2007年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
173
试验地点
1
主要终点
Myocardial infarct size by SPECT

研究概览

简要总结

The purpose of this study to determine whether statin pretreatment decrease myocardial infarct size in patients with acute myocardial infarction undergoing primary percutaneous coronary intervention.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Presence of chest pain for more than 30 minutes but less than 12 hours after symptom onset
  • ST segment elevation more than 1 mm in two or more contiguous leads or presumably a new onset left bundle branch blockage

排除标准

  • Cardiogenic shock
  • History of myocardial infarction
  • Chronic liver disease
  • Previous or current statin use

研究组 & 干预措施

1

Experimental

Atorvastatin group

干预措施: atorvastatin (Drug)

结局指标

主要结局

Myocardial infarct size by SPECT

时间窗: between 5 and 14 days after acute myocardial infarction

次要结局

  • Myocardial infarct size measured by contrast-enhanced MRI(within 14 days after acute myocardial infarction)
  • Myocardial blush grade after the procedure(immediate after procedure)
  • complete ST resolution(at 60 minutes after the procedure)
  • major adverse cardiac events related to left ventricular dysfunction (death, new-onset sustained hypotension or heart failure, and hospital readmission for left ventricular dysfunction)(at 6 months after the procedure)

研究者

申办方类型
Other

研究点 (1)

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