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临床试验/ISRCTN16425597
ISRCTN16425597进行中(未招募)3 期

A Phase III, multi-centre, randomized placebo-controlled trial of oral iron supplementation for the prevention of maternal anaemia

HS Blood and Transplant0 个研究点目标入组 11,020 人开始时间: 2023年11月20日最近更新:
适应症

试验速览

阶段
3 期
状态
进行中(未招募)
发起方
入组人数
11,020

研究概览

简要总结

暂无简介。

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 measured by the first-trimester blood profile) at booking or screening
  • 2. A live fetus on a first-trimester ultrasound scan carried out for viability or dating.
  • 3. 15 weeks + 6 days gestation or less
  • 4. Aged 18 years and above
  • 5. Able to give informed consent and willing to fulfil trial requirements

排除标准

  • 1. Known haemoglobinopathies (women with haemoglobinopathy trait are still eligible)
  • 2. Anaemia of any type, defined by British Society for Haematology guidelines
  • 3. Severe gastrointestinal disease requiring ongoing treatment and potentially 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 30 days

研究者

发起方
HS Blood and Transplant

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