EUCTR2014-000305-13-DE进行中（未招募）1 期
Medically Ill Patient Assessment of Rivaroxaban Versus Placebo IN Reducing Post-Discharge Venous Thrombo-Embolism Risk (MARINER) - MARINER
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 12,000
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
- •The duration of the index hospitalization must have been at least 3 and no more than 10 consecutive days
- •Must meet venous thromboembolism (VTE) risk criteria with a total modified Improve VTE Risk Score of: greater than or equal 4, or 3 with D-dimer > 2*upper limit of normal (ULN), or 2 with D-dimer > 2*ULN
- •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 3400
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 8600
排除标准
- •Any serious bleeding within 3 months prior to randomization or occurring during index hospitalization
- •Serious trauma within 4 weeks before randomization
- •History of hemorrhagic stroke at any time in the past
- •Severe head trauma within 4 weeks of randomization
- •Any medical condition that requires chronic use of any parenteral or oral anticoagulation
研究者
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