跳至主要内容
临床试验/NCT03271450
NCT03271450Unknown不适用

The Dabigatran, Apixaban, Rivaroxaban, Edoxaban, Warfarin Comparative Effectiveness Research Study

Brigham and Women's Hospital1 个研究点 分布在 1 个国家目标入组 416,000 人开始时间: 2017年7月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
入组人数
416,000
试验地点
1
主要终点
Composite Safety Outcome: Intracranial bleed, Gastrointestinal bleed, Other Major bleed

研究概览

简要总结

Approximately half a million Americans annually experience venous thromboembolic disease, including deep venous thrombosis (DVT) and pulmonary embolism (PE). Since 2010, four new oral anticoagulants have been approved for marketing in addition to the vitamin K antagonist warfarin. Very limited head-to-head data exists comparing these treatment options, leaving patients, clinicians, and other stakeholders with little guidance for selecting the best strategy that balances recurrence reduction with risk of bleeding. In the DARE Warfarin CER Study, the researchers compare all five currently available oral anticoagulant agents for the extended treatment of DVT and PE, as well as no extended treatment. This study also aims to evaluate whether treatment heterogeneity exists for specific populations, such as older patients or those with renal dysfunction. In a secondary aim, the study will also leverage a database of linked electronic health record-insurance claims to validate diagnosis definitions and account for potential residual confounding by factors unmeasured in claims data. As the patient population includes all Medicare novel anticoagulant users and large numbers of commercially insured and Medicaid patients, the results will likely be transportable to the majority of US patients experiencing a DVT or PE. Pursuant to the objectives of the Patient-Centered Outcomes Research Institute, a study advisory committee consisting of key stakeholders will be actively involved in the study design and dissemination of results.

研究设计

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

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

  • Any safety outcome between index diagnosis date and index rx date + 90, defined as: intracranial bleed, gastrointestinal bleed, or other major bleed.
  • Any DVT/PE between index diagnosis date and index rx date + 90.

结局指标

主要结局

Composite Safety Outcome: Intracranial bleed, Gastrointestinal bleed, Other Major bleed

时间窗: 1-2 Years

Defined as a new episode of either Intracranial bleed, Gastrointestinal bleed or another Major bleed event during follow-up.

Death

时间窗: 1-2 Years

Measured after index prescription date + 90 days and on date on which the event occurred and defined as hospitalization with discharge status code of: 20, 22-29, 40-42

Composite Effectiveness Outcome: Deep Venous Thrombosis, Pulmonary Embolism

时间窗: 1-2 Years

Defined as a new episode of either Deep Venous Thrombosis or Pulmonary Embolism during follow-up.

Composite safety and effectiveness outcome

时间窗: 1-2 years

defined as earlier of safety or DVT/PE outcomes

Composite safety and effectiveness outcome, including death

时间窗: 1-2 years

Measured after index prescription date + 90 days and on date on which the event occurred and defined as hospitalization with discharge status code of: 20, 22-29, 40-42

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Katsiaryna Bykov, PharmD, ScD

Instructor

Brigham and Women's Hospital

研究点 (1)

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The DARE Warfarin CER Study | 临床试验