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临床试验/IRCT20210730052015N1
IRCT20210730052015N1招募中3 期

Comparison of the effectiveness of treatment of iron deficiency anemia with daily vs. every other day oral iron supplementation

Arak University of Medical Sciences0 个研究点目标入组 376 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
376

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
15 years 至 50 years(—)
性别
Female

入选标准

  • Age = 15 years and less than 50 years
  • outpatients Women with iron deficiency with ferritin less than 30 micrograms per liter
  • No pregnancy
  • No breastfeeding right now
  • Absence of comorbidities (ckd, DM, IHD, etc.)
  • Lack of known history of inflammatory bowel disease
  • Lack of known history of celiac disease
  • No known history or thalassemia
  • No known hereditary bleeding disorder
  • Do not take multivitamin and mineral supplements (35 mg or more of essential iron per day) in the 2 weeks prior to randomization.
  • No allergy to oral iron
  • Lack of intravenous iron therapy in the last 12 weeks
  • Do not receive anticoagulants (eg warfarin, apixaban, debigatran, adoxaban, Riveroxban)
  • Lack of creatinine clearance less than 30 ml per minute
  • Lack of hemoglobin less than 80 g / l with active bleeding
  • No chemotherapy planned for the next 12 weeks.
  • No surgery is scheduled for the next 12 weeks.

排除标准

  • Intolerance or non-response to oral iron gluconate, sulfate or fumarate in the last 12 weeks
  • Received frequent anemia treatments and are resistant to anemia treatment.
  • Dissatisfaction to participate in the study or lack of cooperation and consent to continue treatment

研究者

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