ACTRN12608000186358招募中3 期
Intravenous versus oral iron supplementation for correction of post-transplant anaemia in renal transplant patients
Princess Alexandra hospital (Department of nephrology)0 个研究点目标入组 100 人开始时间: 2008年4月10日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 发起方
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •1.New live or cadaveric donor renal transplant recipient
- •2.Aged 18 years or over
- •3.Able to give written informed consent.
排除标准
- •1.Patients with transferrin saturation >50% or ferritin >800µg/l.
- •2.Women lactating, pregnant or of child-bearing potential not using a reliable contraceptive method.
- •3.Patients with a history of psychological illness or condition which interferes with their ability to understand or comply with the requirements of the study.
- •4.Patients who have received a new investigational drug within the last 4 weeks.
- •5.Intolerance of intravenous or oral iron supplements
- •6.As the following medications can have interactive effects, they cannot be administered during the course of the study:
- •-All new investigational medications
研究者
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