EUCTR2012-003359-12-NL进行中（未招募）不适用
The effect of a high and low protamine-to-heparin dosing on perioperative hemostasis: a randomized clinical trial. - Ratio-PRO study
VU University Medical Center0 个研究点目标入组 98 人开始时间: 2013年8月14日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 98
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Patients undergoing coronary artery bypass graft (CABG) surgery.
- •Age 18-85 years
- •Informed consent
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 28
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 70
排除标准
- •Re-operations
- •Emergency operation
- •Patients with a history of hematologic disorders or renal replacement therapy.
- •Patients with a body mass index (BMI) below 18 kg/m2 or above 35 kg/m2
研究者
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