NL-OMON21605招募中不适用
Validation of a new fibrinolysis assay for thrombelastometry on the ROTEM® device
MUMC+0 个研究点目标入组 200 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 200
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
入选标准
- •The population consist of all in hospital adult (= 18 years old) patients at the Maastricht University Medical Centre. 20-30 patients of each group will be asked informed consent for blood withdrawal for this in vitro measurement on the ROTEM® device.
- •The population consist of the following patient groups:
- •- Sepsis (with/without DIC)
- •- Liver impairment (Child-Pugh A/B/C)
- •- Patientgroups in which an altered hemostatic balance can be expected, like patients treated for hematological malignancies who have severe thrombocytopenia
排除标准
- •temperature >38,0°C, sepsis, active bleeding, splenomegaly or use of anticoagulation medication.
研究者
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