ISRCTN51513145已完成未知
A randomised controlled pilot study comparing standard fluid management with haemoconcentration of remaining cardiopulmonary bypass blood using the new Hemosep device
Papworth Hospital NHS Trust (UK)0 个研究点目标入组 60 人开始时间: 2014年2月18日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 60
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
- •Adult patients undergoing elective or urgent coronary artery bypass graft surgery (CABG), heart valve surgery, or a combination of CABG and valve surgery will be included.; Target Gender: Male & Female ; Lower Age Limit 18 years
排除标准
- •1. Patients under 18 years of age
- •2. Patients undergoing emergency surgery
- •3. Patients with a contraindication to either heparin, protamine or tranexamic acid
- •4. Patients who might not adequately understand verbal explanations or written information given in English, or who have special communication needs
研究者
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