ACTRN12610000876099终止未知
A Randomised Controlled Trial in Adult Patients Undergoing Coronary Artery Bypass Graft Surgery Designed to Determine the Optimal Dose for Remote Ischaemic Preconditioning Compared to No Remote Ischaemic Preconditioning and Measuring the Primary Outcome of Area Under the Curve for Troponin to 72 hours Post Aortic Cross Clamp Removal.
适应症
试验速览
- 阶段
- 未知
- 状态
- 终止
- 入组人数
- 96
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Prevention
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 85 Years（—）
- 性别
- All
入选标准
- •Undergoing coronary artery bypass graft surgery with cardiopulmonary bypass
排除标准
- •1. documented ejection fraction <50%,
- •2. concurrent valvular surgery,
- •3. myocardial infarction within 21 days,
- •4. possible radial artery harvesting,
- •5. planned cross-clamp fibrillation,
- •6. >85 years of age,
- •7. peripheral vascular disease affecting the upper limbs
- •8. taking the sulphonylurea glibenclamide
研究者
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