CTRI/2019/08/020863尚未招募未知
A randomized controlled trial comparing the efficacy, tolerability and cost of oral iron preparations in iron deficiency anemia in pregnancy
il0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
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
- •1.Pregnant women with age between 20 and 40 years and period of gestation from 12 to 30 weeks.
- •2.Hemoglobin ranging from 7 to 10.5 g% at the start of the study
- •3.Treatment naïve patients
- •4.Singleton pregnancy
- •5.Patients willing to give written informed consent
排除标准
- •1.Pregnant women with any other types of anemia such as megaloblastic anemia, thalassemia, sickle cell anemia, anemia of chronic disease, hemolytic anemia and anemia due to chronic blood loss.
- •2.Pregnant women with Hb <7 g% & Hb >10.5g%
- •3.Pregnant women with known hypersensitivity to iron preparations
- •4.Pregnant women with any other comorbidities such as renal or hepatic impairment, cardiovascular diseases, preeclampsia, GDM, thyroid disorders, acid peptic disease, esophagitis and malabsorption syndrome.
- •5.Treatment with any other investigational drug in the last 1 month before study entry
- •6.Multiple pregnancy
研究者
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