ISRCTN21955180已完成未知
A double-blind randomised controlled trial comparing standard dose of iron supplementation for pregnant women with two screen-and-treat approaches using hepcidin as a biomarker for ready and safe to receive iron
The Medical Research Council (MRC) (UK)0 个研究点目标入组 498 人开始时间: 2014年4月14日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 498
研究概览
简要总结
- 2016 protocol in: https://www.ncbi.nlm.nih.gov/pubmed/27411564 2. 2019 results in https://www.ncbi.nlm.nih.gov/pubmed/31607468 (added 15/10/2019)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- Female
入选标准
- •1. Pregnant (gestational age between 14 - 22 weeks)
- •2. Age: 18 to 45 years
- •3. Likely to be resident in study area for duration of trial
- •4. Written informed consent obtained
排除标准
- •1. Severely anaemic (< 7 g/dl)
- •2. Seriously ill (infectious disease of clinical significance) at recruitment
- •3. Chronic disease
- •4. Pregnancy complications (e.g. pre-eclampsia) at enrolment
- •5. Already part of another study
研究者
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