跳至主要内容
临床试验/NCT01402739
NCT01402739终止不适用

Monocentric Pilot Study of Algorithm-Guided Transfusions in Cardiac Surgery Patients for Reduction of Drainage Blood Losses

Michael Sander1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2011年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
发起方
入组人数
100
试验地点
1
主要终点
chest tube output

研究概览

简要总结

Cardiac surgery patients have a risk to need allogeneic blood transfusions that depends on several risk factors, e.g. the type of surgery, concomitant medication with anticoagulants, and postoperative chest tube output. Allogeneic blood transfusion is associated with transfusion reactions, infection transmission, and postoperative morbidity and mortality. The aim of this study is to investigate, whether cardiac surgery patients have a reduced postoperative chest tube output and transfusion need when using a point-of-care guided transfusion algorithm compared to standard of care transfusion protocols.

详细描述

Cardiac surgery patients have a risk to need allogeneic blood transfusions that depends on several risk factors, e.g. the type of surgery, concomitant medication with anticoagulants, and postoperative chest tube output. Allogeneic blood transfusion is associated with transfusion reactions, infection transmission, and postoperative morbidity and mortality. The aim of this study is to investigate, whether cardiac surgery patients have a reduced postoperative chest tube output and transfusion need when using a point-of-care guided transfusion algorithm compared to standard of care transfusion protocols .

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

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •elective cardiac surgery patient requiring cardiopulmonary bypass
  • •moderate or high transfusion risk
  • •signed informed consent

排除标准

  • •age <18 or >80 years
  • •known hemophilia
  • •known thrombophilia
  • •known thrombocytopathy
  • •hereditary or acquired coagulation disorder
  • •active endocarditis
  • •ejection fraction <30%
  • •BSA < 1.8 sqm
  • •planned aortic arch surgery
  • •preoperative thrombocytopenia <150/nl
  • •underlying hemostaseological disease
  • •preoperative anemia
  • •liver cirrhosis Child B or higher
  • •preoperative creatinine > 2mg/dl
  • •terminal renal insufficiency requiring dialysis
  • •vitamin k antagonists during 5 days prior to surgery
  • •pregnant or breast-feeding women
  • •known allergy against allogeneic blood products or coagulation factors
  • •refusal of blood transfusions
  • •any concomitant investigational agent or participation in another trial

研究组 & 干预措施

PoC algorithm guided transfusions

Experimental

experimental arm

干预措施: Point of Care Coagulation Monitoring Guided Transfusion Algorithm (Other)

standard of care transfusions

Active Comparator

control arm

干预措施: standard coagulation monitoring guided transfusion algorithm (Other)

结局指标

主要结局

chest tube output

时间窗: 24 hours

次要结局

  • course of conventional coagulation parameters (aPTT, TPZ, fibrinogen, FXIII, ACT)(24 hours)
  • incidence of RRT(during 30 days)
  • duration of mechanical ventilation(hours (average))
  • need of allogeneic blood transfusions(24 hours)

研究者

发起方
Michael Sander
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Michael Sander

Univ.-Prof. M. Sander

Charite University, Berlin, Germany

研究点 (1)

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