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临床试验/NCT01619007
NCT01619007已完成不适用

Xarelto® for Long-term and Initial Anticoagulation in Venous Thromboembolism (VTE)

Bayer0 个研究点目标入组 5,145 人开始时间: 2012年6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
5,145
主要终点
All cause mortality

研究概览

简要总结

Following the findings of the clinical trials in drug development, this global non-interventional cohort field study will investigate rivaroxaban under clinical practice conditions in comparison with current standard of care for patients with acute deep vein thrombosis (DVT).

The main goal is to analyze long-term safety in the use of rivaroxaban in the treatment of acute DVT in routine clinical practice.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • Female and male patients
  • Patients >= 18 years
  • Patiebts with diagnosis of acute DVT and who have an indication for anticoagulation therapy for at least 12 weeks, who are willing to participate in this study and are available for follow-up

排除标准

  • Exclusion criteria must be read in conjunction with the local product information.

研究组 & 干预措施

Group 1

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

Group 2

干预措施: Standard of care (Drug)

结局指标

主要结局

All cause mortality

时间窗: after approximately 2 years or 30 days after stop of therapy

Number of patients with symptomatic recurrent venous thromboembolic events

时间窗: after approximately 2 years or 30 days after stop of therapy

Major bleedings defined as overt bleeding associated with: A fall in hemoglobin of ≥2 g/dL; or a transfusion of ≥2 units of packed red blood cells or whole blood; or occurrence at a critical site

时间窗: after approximately 2 years or 30 days after stop of therapy

次要结局

  • Treatment satisfaction (patient reported outcomes)(after approximately 2 years or 30 days after stop of therapy)
  • Safety variables will be summarized using descriptive statistics based on adverse cardiac events collection(after approximately 2 years or 30 days after stop of therapy)
  • Number of patients with other symptomatic thromboembolic events(after approximately 2 years or 30 days after stop of therapy)

研究者

发起方
Bayer
申办方类型
Industry
责任方
Sponsor

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