NCT02512250招募中不适用
Swiss Hemophilia Registry
Swiss Hemophilia Network19 个研究点 分布在 1 个国家目标入组 900 人开始时间: 2015年5月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 900
- 试验地点
- 19
- 主要终点
- Number of incidence of disease and inhibitor development
研究概览
简要总结
The Swiss Hemophilia Registry will collect data on the prophylactic and therapeutic use of factor concentrates in patients with hemophilia and other severe bleeding disorders in Switzerland.
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
- •Diagnosis of hemophilia or other severe bleeding disorders. Signed inform consent
排除标准
- 未提供
结局指标
主要结局
Number of incidence of disease and inhibitor development
时间窗: 1 year
Demographics, Comorbidties, factor consumption for prophylaxis, bleeding and surgery, inhibito develeopment
次要结局
未报告次要终点
研究者
研究点 (19)
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