ISRCTN12911644已完成Unknown
A pilot clinical trial to test the acceptability and feasibility of different doses of oral iron supplementation to prevent maternal anaemia - PANDA-Dose Study
HS Blood and Transplant0 个研究点目标入组 300 人开始时间: 2023年4月27日最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 发起方
- 入组人数
- 300
研究概览
简要总结
2024 Results article in https://pubmed.ncbi.nlm.nih.gov/39208353/ (added 02/09/2024)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- Female
入选标准
- •1. Healthy non-anaemic pregnant women of all parities (haemoglobin concentration (Hb) > = 110 g/l) at booking or screening.
- •2. 13 weeks + 6 days gestation or less
- •3. Age 18 and above
- •4. Able to give informed consent and willing to fulfil trial requirements
排除标准
- •Women with the following conditions will be excluded:
- •1. Known haemoglobinopathies
- •2. Anaemia of any type, defined by BSH guidelines
- •3. Severe gastrointestinal disease, affecting tolerability of oral iron
- •4. Allergies to iron
- •5. Multiple pregnancies, given the higher iron demands
- •6. Known haemochromatosis
- •7. Recent red cell transfusion, within 1 month
研究者
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