ACTRN12612001249842进行中（未招募）2 期
For patients with anaemia admitted to the Intensive Care Unit, does intravenous iron compared with placebo reduce red blood cell transfusion requirement?
Edward Litton0 个研究点目标入组 140 人开始时间: 2012年11月26日最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 140
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
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •1.Admitted to an ICU for less than 48 hours
- •2.Anticipated to require ICU care beyond the next calendar day
- •3.Hb less than 100 g/L at any time during the preceding 24 hours
- •4.Age 18 years or greater
排除标准
- •1.Suspected or confirmed severe sepsis (two or more Systemic Inflammatory Response Syndrome (SIRS) criteria, suspected or confirmed infection, and one or more organ system failure)
- •2.Serum ferritin greater than 1200ng/ml or transferrin saturation greater than 50%
- •3.History of haemochromatosis or aceruloplasminaemia
- •4.Known prior administration of IV iron in the preceding 3 months
- •5.Jehovah’s Witness or other documented exclusion to receiving blood products
- •6.Receiving ESA (e.g. epoetin or darbepoeitin) in the 3 months prior to ICU admission
- •7.Known hypersensitivity to intravenous iron
- •8.Pregnancy
- •9.Treatment intent is palliative
- •10.Death is deemed imminent and inevitable
- •11.Weight less than 40kg
- •12.Participating in competing study
研究者
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