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临床试验/NCT03749057
NCT03749057已完成4 期

Early Rivaroxaban for Acute Ischemic Stroke or TIA Patients With Atrial Fibrillation: a Prospective, Multicenter, Cohort Study

General Hospital of Shenyang Military Region1 个研究点 分布在 1 个国家目标入组 400 人开始时间: 2018年11月20日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
400
试验地点
1
主要终点
incidence of intracranial hemorrhage

研究概览

简要总结

Anticoagulant treatment for non-valvular atrial fibrillation (AF) associated with cerebral infarction/ TIA is one of the recognized treatment of stroke prevention. The ACC/AHA and national guidelines for the management of anticoagulation recommend that most of AF patients with cerebral infarction or TIA should be administrated anticoagulant therapy within 14 days of symptom onset, while European guidelines recommend that the timing of the initiation of non-vitamin K antagonist oral anticoagulants (NOACs) for AF patients with cerebral infarction or TIA is association with stroke severity in light of the "1-3-6-12" principle. However, there are still many problems about the use of NOACs in ischemic stroke with AF. for example, it is unclear what time to begin NOACs as to difference in stroke severity, ages, comorbidity with hypertension, diabetes, heart failure, liver and kidney dysfunction and bleeding risks. Thus, the timing of the initiation of NOACs is yet to be further studied. Current urgent need is to develop a guideline-based specific regimen in which the benefit-risk factors are further balanced with a combination of NHISS, CHA2DS2-VASC and HAS-BLED score.

Rivaroxaban, a direct coagulation factor Ⅹa inhibitor, blocks the formation of the clot. ROCKET-AF study has shown that the efficacy of rivaroxaban is not inferior to that of warfarin in AF patients on stroke prevention, and rivaroxaban has a significantly decreased bleeding risk compared with warfarin. Recent study indicates that early administration with rivaroxaban for AF patients within 14 days of onset does not significantly increase hemorrhagic transformation. However, the relevant clinical data of the efficacy and safety of early initiation of rivaroxaban in AF patients with cerebral infarction or TIA are lacking in China.

Therefore, the investigators conduct a multicenter cohort study to investigate the safety of early rivaroxaban in the AF patient with cerebral infarction or TIA within 12 days of onset.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • Hemorrhagic stroke or mixed stroke
  • Patients with valvular atrial fibrillation or non-cardiogenic cerebral infarction
  • Patients with severe infection or serious diseases
  • Gastrointestinal bleeding or major operation within 3 months
  • Planed cerebrovascular reconstruction or cardiac surgery within 3 months
  • Planed major surgery within 3 months
  • Participating in other clinical trials within 3 months
  • Unsuitable for this trial assessed by research

研究组 & 干预措施

rivaroxaban

Other

15-20 mg rivaroxaban daily

干预措施: Rivaroxaban (Drug)

结局指标

主要结局

incidence of intracranial hemorrhage

时间窗: 7 days

次要结局

  • recurrence of stroke or other vascular events(90 days)
  • bleeding event(90 days)
  • incidence of early neurological deterioration(7 days)
  • Serious adverse events(90 days)

研究者

发起方
General Hospital of Shenyang Military Region
申办方类型
Other
责任方
Principal Investigator
主要研究者

Hui-Sheng Chen

Department Chairman

General Hospital of Shenyang Military Region

研究点 (1)

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