DRKS00017369已完成不适用
A Prospective, Non-Interventional Study to investigate the Effectiveness of AFSTYLA® in Patients with Hemophilia A - not applicable
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 52
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
- 年龄范围
- one 至 one（—）
- 性别
- All
入选标准
- •The treatment decision was made by the attending physician in accordance with standard medical practice and independently of this study
- •Written and personally dated consent of the patient or for minors of the legal representative after a detailed explanation of the observational study by the attending physician. The consent must correspond to the presumed will of the minor, if one can be determined. The underage patient should also be given the opportunity to consent in writing, provided that his / her age allows to do so according to the physician
- •diagnosed with Hemophilia A
- •treatment with AFSTYLA® according to the medical practice and the latest product information for the treatment and prevention of bleeding events
排除标准
- •currently participating in a clinical trial
- •known hypersensitivity to the active substance or other ingredients
- •known allergic reaction to hamster proteins
- •presence of inhibitors to FVIII or to AFSTYLA® (from = 0,6 BE /ml) and/or immune tolerance treatment at the time of recruitment
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