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临床试验/CTRI/2021/05/033579
CTRI/2021/05/033579尚未招募未知

To study safety and efficacy of intravenous iron ferric-carboxymaltose in iron deficiency anaemia of pregnancy

DST Chandigarh0 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.Hemoglobin levels of >= 6 gm/dl - 9 gm/dl
  • 2. Diagnosed case of Iron deficiency anemia.
  • 3. Period of gestation between 20 to 36 weeks.
  • 4. Singleton live pregnancy

排除标准

  • 1.Anemia other than iron deficiency anemia.
  • 2.Known serious hypersensitivity to other parenteral iron products.
  • 3.Patients with known allergies including drug allergies, including patients with a history of severe asthma, eczema or other atopic allergy.
  • 4.Patients with immune or inflammatory conditions (e.g. systemic lupus erythematosus, rheumatoid arthritis).
  • 5.Chronic medical disorder
  • 7.Antepartum hemorrhage
  • 8.Anemia with heart failure
  • 9. H/O Blood transfusion during current pregnancy.
  • 11.COVID positive patient

研究者

发起方
DST Chandigarh

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