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临床试验/IRCT20231023059817N4
IRCT20231023059817N4尚未招募3 期

Comparing the therapeutic effects of two methods of injectable iron and oral iron on quality of life, sleep quality, and breastfeeding self-efficacy in women with iron deficiency/ iron deficiency anemia in the postpartum period (postpartum)

Zistaroo Danesh Company0 个研究点目标入组 170 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
170

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

年龄范围
18 years 至 no limit(—)
性别
Female

入选标准

  • Mothers who have hemoglobin between 9 and 10.5 g/dl after giving birth.
  • Having informed consent

排除标准

  • History of anemia due to reasons other than iron deficiency and blood loss during pregnancy or being pregnant
  • The presence of more bleeding than usual postpartum (after the first 24 hours, more than menses or passing a large clot)
  • Severe active infection
  • Having a history of allergy to injectable iron
  • The presence of systemic disease in the mother (patients who received erythropoiesis stimulator (erythropoietin) during the last 3 months, patients who received myelosuppressive treatment and blood or blood products during delivery, patients with asthma under treatment, patients with hepatitis, Patients with HIV, patients with blood problems other than iron deficiency, patients with IBD, patients with CKD (eGFR<60)
  • Having a history of sleep disorder or depression and mothers who need to receive antidepressants.
  • Mothers who have suffered the death of a fetus or baby
  • Taking PPI, H2 blocker and antihistamine

研究者

发起方
Zistaroo Danesh Company

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