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临床试验/SLCTR/2022/005
SLCTR/2022/005招募中4 期

EdoxabaN foR IntraCranial Hemorrhage survivors with Atrial Fibrillation

Hamilton Health Sciences, through its Population Health Research Institute0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Age greater than or equal to 45 years, at the time of signing the informed consent
  • Previous intracranial hemorrhage (symptomatic, spontaneous and non-traumatic intraparenchymal, intraventricular, and/or Convexal subarachnoid hemorrhage cSAH, and symptomatic spontaneous or non-penetrating traumatic subdural hemorrhages) on or off antithrombotic therapy (Table 2)
  • Documented atrial fibrillation (paroxysmal, persistent, permanent)
  • CHA2DS2-VASc score greater than or equal to 2

排除标准

  • Recent intracranial hemorrhage (within 14 days)
  • Secondary macrovascular, neoplastic or infectious causes of intracranial hemorrhage (except for antithrombotic treatment or non-penetrating traumatic subdural hemorrhages)
  • Traumatic or aneurysmal cSAH
  • Need for ongoing oral anticoagulant therapy for indication other than AF (e.g. mechanical heart valve, venous thromboembolic disease)
  • Need for ongoing antiplatelet therapy for indication where edoxaban would not be a suitable substitute
  • Plans for left atrial appendage occlusion
  • Estimated creatinine clearance (CrCl) < 15 mL/min or other creatinine clearance following local product monograph (Canada < 30mL/min)
  • Platelet count less than 100,000mm3 at enrollment or other bleeding diathesis
  • Persistent, uncontrolled hypertension (systolic BP averaging >150 mmHg)
  • Chronic use of NSAID
  • Clinically significant active bleeding, including gastrointestinal bleeding
  • Lesions or conditions at increased risk of clinically significant bleeding, e.g. active peptic ulcer disease with recent bleeding, patients with spontaneous or acquired impairment of hemostasis
  • Antiphospholipid antibody syndrome
  • Hepatic disease associated with coagulopathy and clinically relevant bleeding risk
  • Known hypersensitivity to edoxaban
  • Estimated inability to adhere to study procedures
  • Pregnancy or breastfeeding
  • Estimated life expectancy < 6 months at the time of enrollment
  • Close affiliation with the investigational site; e.g. a close relative for the investigator, dependent person (e.g., employee or student of the investigational site)

研究者

发起方
Hamilton Health Sciences, through its Population Health Research Institute

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