EUCTR2009-010623-64-SE进行中（未招募）不适用
A clinical open, randomised study of oral iron (Duroferon®) vs. intravenous iron (Ferinject®) for iron substitution in blood donors.
Renapharma AB0 个研究点目标入组 210 人开始时间: 2009年2月19日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 210
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Males and females qualified as whole blood donors .
- •Fulfilled at least 5 previous whole blood donations.
- •Signed informed consent.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Anaemia not attributable to iron deficiency, e.g. other type of microcytic anaemia.
- •Iron overload.
- •Contraindications for Ferinject® or Duroferon®.
- •Contraindications for blood donations.
研究者
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