ISRCTN11568655进行中（未招募）未知
on-interventional study to capture data on the use of a VWF/FVIII concentrate (wilate®) in all clinical settings of von Willebrand disease including health-related quality of life
试验速览
- 阶段
- 未知
- 状态
- 进行中（未招募）
- 入组人数
- 120
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
- 性别
- All
入选标准
- •1. The patient has congenital or acquired Von Willebrand disease (VWD) and requires injections with VWF-containing concentrate (wilate)
- •2. With a positive bleeding history, other possible causes have been excluded
排除标准
- •1. Patients with known contraindications as specified in the Summary of Product Characteristics (SPC)
- •2. The patient could actually be treated with DDAVP (Desmopressin Acetate)
- •3. The patient has a von Willebrand factor activity over 70% and there are no findings manifesting the VWD diagnosis
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