NL-OMON37417已完成不适用
The efficacy of pro- and anticoagulant therapy in plasma from patients with liver cirrhosis . - EPAC
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 126
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
- •Inclusion criteria study group:
- •- Cirrhosis
- •- >18 year
- •- Signed informed consent
- •Inclusion criteria healhty control group
- •- >18 year
- •- Signed informed consent
排除标准
- •Exclusion criteria study group:
- •- Congenital coagulation disorder
- •- Active infection
- •- Acute liver failure
- •- Use of anticoagulant drugs in the past 10 days
- •- Pregnancy
- •- (<7 days) transfusion with blood products;Exclusion criteria control-group
- •- Documented history of congenital coagulation disorder
- •- History of vascular disease
- •- History of hepatic disease
- •- History of any systemic disease
- •- Recent viral infection (>2 weeks)
- •- Use of anticoagulant drugs in the past 10 days
- •- Pregnancy
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