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临床试验/NCT02262676
NCT02262676已完成不适用

Observational and Cross-sectional Study to Assess the Sociodemographic and Clinical Characteristics of Patients Treated With RIVAROXABAN in the Context of Routine Clinical Practice of Spanish Haematologists, Cardiologists and Internists (HEROIC Study)

Bayer0 个研究点目标入组 2,251 人开始时间: 2014年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
Bayer
入组人数
2,251
主要终点
Medical History

研究概览

简要总结

Depict demographic and clinical features of patients with atrial fibrillation treated with rivaroxaban to prevent stroke and pulmonary embolism in routine clinical practice

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

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

  • Patients ≥ 18 years
  • Patients with atrial fibrillation
  • Patients in treatment with rivaroxaban for stroke prevention in atrial fibrillation at least 3 months previous to inclusion period in study

排除标准

  • Patients in treatment after start of study
  • Patients treated with other anticoagulant treatment

研究组 & 干预措施

Rivaroxaban

Patients with Atrial fibrillation treated with Rivaroxaban

干预措施: Rivaroxaban (Xarelto, BAY59-7939) (Drug)

结局指标

主要结局

Medical History

时间窗: At recruitment visit

Demographic Data

时间窗: At recruitment visit

次要结局

  • Assess the quality of life in patients(At recruitment visit)
  • Assess regional differences among the different Spanish autonomous communities on the management of patients with rivaroxaban treatment during the routine clinical practice(At recruitment visit)
  • Adherence to rivaroxaban treatment(At recruitment visit)
  • Assess the satisfaction of rivaroxaban treatment(At recruitment visit)

研究者

发起方
Bayer
申办方类型
Industry
责任方
Sponsor

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