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临床试验/IRCT20200112046094N1
IRCT20200112046094N1招募中3 期

Aspirin plus Rivaroxaban Efficacy and Safety in Embolic Stroke of Undetermined Source: A Randomized, Placebo Controlled, Outcome Assessor Blind, Clinical Trial

Mazandaran University of Medical Sciences0 个研究点目标入组 40 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
40

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

年龄范围
18 years 至 no limit(—)
性别
All

入选标准

  • Signing the informed consent
  • Recent ischemic stroke, with criteria of ESUS defined as:Stroke detected by CT or MRI that is not lacunar,Absence of extracranial or intracranial atherosclerosis causing =50% luminal stenosis in arteries supplying the area of ischemia, No major-risk cardioembolic source of embolism, No other specific cause of stroke identified
  • only one risk factor of potential embolic source including:PTFV1 in standard ECG =0.05 mm.s or =0.005 mv.s,LVH in standard ECG( Sokolow index= 35 mm), Moderate or severe MR, AR or AS in echocardiography , LVH in echocardiography, left atrium hypertrophy in echocardiography, PFO not candidate for closure

排除标准

  • History of hypersensitivity to the investigational medicinal product
  • Indication for anticoagulation
  • Indication for dual antiplatelet therapy
  • Contraindication to investigational medications
  • History of intracranial, intraocular, spinal, retroperitoneal or atraumatic intra-articular bleeding
  • Gastrointestinal bleeding or major surgery within 3 months
  • Planned or likely revascularization (any angioplasty or vascular surgery) within the next 3 months
  • HAS-BLED score > 3
  • Severe non-cardiovascular comorbidity with life expectancy < 3 months
  • Severe renal failure, defined as Glomerular Filtration Rate (GFR) <15ml/min, Dialysis, transplant, Cr >2.26 mg/dL
  • Severe hepatic insufficiency, Cirrhosis or Bilirubin >2x Normal or AST/ALT/AP >3x Normal
  • Modified Rankin Scale of >=4
  • Inability to swallow medications
  • Hemorrhagic transformation of infarction

研究者

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