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临床试验/IRCT20210503051166N2
IRCT20210503051166N2尚未招募3 期

The evaluation of the effect of administration time of oral Iron preparations on hemoglobin response in patients with Iron deficiency anemia

Mashhad University of Medical Sciences0 个研究点目标入组 196 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
入组人数
196

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 75 years(—)
性别
All

入选标准

  • Patients with iron deficiency anemia based on iron profile study such as serum iron, ferritin, and transferrin saturation percent
  • Hemoglobin level less than 11 mg/dl
  • Not suffering from chronic liver disease (normal bilirubin, LFT<2 times normal), or other chronic inflammatory diseases based on initial evaluation
  • Not suffering from active malignancy based on initial evaluation
  • Not suffering from active infection based on initial evaluation
  • Not suffering from any of the malabsorption syndromes based on the initial evaluation
  • Patients with cardiovascular risk factors

排除标准

  • Suffering from any chronic kidney disease, liver disease, all types of cancer, infections and autoimmune diseases
  • The patient's lack of consent to participate in the plan
  • Having dyspepsia and intolerance to iron food products
  • High CRP levels at study entry

研究者

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