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临床试验/EUCTR2014-000305-13-DK
EUCTR2014-000305-13-DK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

Janssen-Cilag International NV0 个研究点目标入组 8,000 人开始时间: 2014年5月21日最近更新:
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
8,000

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 2700
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 5300

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 3 months of randomization
  • Any medical condition that requires chronic use of any parenteral or oral anticoagulation

研究者

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