NL-OMON51243尚未招募4 期
The efficacy of intermittent versus daily oral iron supplementation in anaemic pregnant women. - FER-IDIP trial (FER Intermittent vs Daily In Pregnancy)
适应症
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 入组人数
- 58
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
入选标准
- •- Pregnant women of 18 years and older
- •- Iron deficiency anaemia (defined as: Anaemia (haemoglobin lower than cut-off
- •value) AND mean corpuscular volume (MCV) 70-85 fl OR ferritin <30ug/L) OR mean
- •corpuscular volume (MCV) < 70fl / hemoglobinopathy is ruled out.
- •- Adequate mental health
- •- Good command of the Dutch language
- •- No participation in other research with medication
- •- Informed consent
排除标准
- •- Start of iron supplementation at pregnancy duration > 37 weeks (because of
- •the limited time to achieve an increase in haemoglobin).
- •- History of bariatric surgery, inflammatory bowel disease, coeliac disease or
- •Helicobacter pylori infection (because of malabsorption of iron).
- •- Patients who received blood transfusion or parental iron supplementation
- •during the 3 months prior to screening (because of the effect on the
- •haemoglobin level).
- •- Patients with significant bleeding, blood donation or surgery during
- •pregnancy (because of the effect on the haemoglobin level).
- •- Allergy for iron.
- •- Anaemia of other cause, such as a hemoglobinopathy.
研究者
相似试验
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