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临床试验/EUCTR2005-005040-85-AT
EUCTR2005-005040-85-AT进行中(未招募)不适用

Comparison of Albumin 5%, Hydroxyethyl Starch 130/0.4 (6%) and Ringer Lactate for volume replacement during cardiac surgery - n/a

Department of Anesthesia, Div. of Cardiothoracic and Vascular Anesthesia, Medical University Vienna0 个研究点目标入组 240 人开始时间: 2006年2月1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
240

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

  • 1) Patients undergoing elective cardiac surgery using cardiopulmonary bypass including coronary artery bypass grafting (CABG), valve repair or replacement, and Aorta ascendens surgery
  • 2) Age > 18 years
  • 3) Written informed consent obtained
  • 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
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1) Known allergy to Hydroxyethyl starch or Albumin
  • 2) Aspirin use less than 3 days before surgery
  • 3) GPIIbIIIa antagonists use less than 7 days before surgery
  • 4) Coagulation disorders (INR > 1.2, aPTT > 40sec, platelet count < 100.000)
  • 5) BMI > 40
  • 6) Left ventricular ejection fraction < 15%
  • 7) Renal dysfunction defined as serum creatinine >1.5mg/dl
  • 8) Proven heparin induced thrombocytopenia (Danaparoid, Lepirudin use less than 1 month)
  • 9) Deny of consent

研究者

发起方
Department of Anesthesia, Div. of Cardiothoracic and Vascular Anesthesia, Medical University Vienna

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Comparison of Albumin 5%, Hydroxyethyl Starch... | 临床试验