NL-OMON49798已完成不适用
Haemophilia in the Netherlands 6 - HiN-6
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 1,250
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
- 2 至 64（—）
入选标准
- •- Men with severe, moderate, mild congenital haemophilia A or B that are
- •registered at one of the haemophilia treatment centres in the Netherlands.
- •- Written informed consent before data collection and sampling blood/urine.
- •- Male patients with congenital haemophilia A or B who underwent liver
- •transplantation in the past (irrespective of their endogenous clotting factor
- •- All currently deceased male haemophilia A or B patients that participated in
- •the HiN-5 questionnaire in 2001
排除标准
- •- Female carriers of haemophilia A or B
- •- Symptomatic carriers of haemophilia A or B
- •- Patients with acquired haemophilia.
- •- Patients with reduced FVIII levels due to Von Willebrand disease.
- •- Inability to obtain informed consent from patients older than 12 years of age.
- •- No informed consent before data collection and sampling blood/urine.
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