ACTRN12612000423819尚未招募4 期
An evaluation of adverse events and haemodynamic instability resulting from the rapid administration of iron polymaltose infusion in the operating department, in patients with iron deficiency anaemia under general anaesthesia for elective surgical procedures.
Fremantle Hospital0 个研究点目标入组 100 人开始时间: 2012年4月16日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 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
- Non-randomised trial
- 主要目的
- Treatment
入排标准
- 年龄范围
- 18 Years 至 100 Years（—）
- 性别
- All
入选标准
- •Iron deficiency anaemia defined as Hb < 120g/L if female or Hb < 130g/L if male with ferritin < 100 or Iron deficiency alone, defined as ferritin < 30
- •Elective surgery / procedure requiring general anaesthesia
排除标准
- •Iron overload (haemochromatosis or haemosiderosis) or ferritin > 100
- •Clinically significant renal or liver disease
- •Chronic polyarthritis
- •Active infection
- •Allergy / intolerance to iron polymaltose
研究者
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