临床试验/CTRI/2019/09/021158

CTRI/2019/09/021158进行中（未招募）4 期

A Real-World, Prospective, Observational Study to Evaluatethe Safety and Effectiveness of Rivaroxaban (XareltoÂ®) forPrevention of Stroke and Systemic Embolism in IndianPatients with Non-valvular Atrial Fibrillation (NVAF) - XARI

Bayer Zydus Pharma Private Limited0 个研究点目标入组 0 人开始时间: 待定最近更新: 2023年4月3日

试验速览

阶段: 4 期
状态: 进行中（未招募）
发起方: Bayer Zydus Pharma Private Limited

研究概览入排标准研究者记录与标识符相似试验

研究概览

简要总结

暂无简介。

研究设计

研究类型: Observational

入排标准

入选标准

•Patient should be an adult female or male, >=18 years of age;
•Patient should be diagnosed with NVAF and initiated with rivaroxaban treatment for
•prevention of stroke or systemic embolism per investigatorâ??s routine treatment practice;
•Patient should not have received rivaroxaban in the past;
•Patient/patientâ??s legally acceptable representative should be willing to provide written
•informed consent.

排除标准

•1. Patient has contraindications to receive rivaroxaban therapy according to local prescribing
•information;
•2. Patient is receiving anticoagulant therapy for indication other than NVAF and that needs to
•be continued as per discretion of treating physician;
•3. Patient is participating in an investigational program with interventions outside of routine
•clinical practice.

研究者

发起方

Bayer Zydus Pharma Private Limited

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