NL-OMON45881撤回不适用
Apheresis based treatment of sepsis - ASSIST
适应症
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 入组人数
- 15
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •Volunteers:
- •- >18 years old
- •- Healthy male volunteer
- •- Meet eligibility criteria for donating whole blood in the Netherlands
- •- Informed consent;Patients:
- •- ICU patient recovering from sepsis, who have detectable RBC-pathogen complexes in their blood.
- •- * 18 years old
- •- Existing vascular access preferably a double lumen dialysis catheter
- •- Informed consent
排除标准
- •Volunteers:
- •- Any abnormal test result during the screening prior to inclusion of the study (medical history, physical examination, and blood examination)
- •- History of drugs or alcohol abuse
- •- Any present medication use on prescription
- •- Participation in any other intervention study during the course of this study;Patients:
- •- Hemodynamic instability as defined by requiring >0.1 mcg/kg/minute of norepinephrine to reach a MAP of > 60 mmHg.
- •- Active bleeding as assessed by the treating physician
- •- Haematological disorders.
- •- Pregnant or lactating women
研究者
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