NCT07101224已完成不适用
Data Registry in Chinese Hemophilia A and B Patients Related to the Use of Anti-hemophilic Coagulation Factor Replacement Therapy
Institute of Hematology & Blood Diseases Hospital, China1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2017年5月7日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 200
- 试验地点
- 1
- 主要终点
- The incidence of MIEs and other SAEs
研究概览
简要总结
This is an open-label, prospective, multi-center, patient registry in Chinese Hemophilia A and B patients treated with anti-hemophilic coagulation factor replacement therapy.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- •Unwilling or unable to follow the terms of the protocol.
结局指标
主要结局
The incidence of MIEs and other SAEs
时间窗: at the end of 2 year data registry
The incidence of MIE(medically important events)s and other SAE(serious adverse event)s in the anti-hemophilic replacement treatment
次要结局
- Treatment regimen(at the end of 2 year data registry)
研究者
研究点 (1)
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