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临床试验/PACTR202404915122192
PACTR202404915122192已完成4 期

A comparative study to evaluate the efficacy and tolerability of new generations of iron preparations with traditional iron therapy in pediatrics: A prospective randomized controlled trial.

Menoufia faculty of medicine0 个研究点目标入组 87 人开始时间: 2024年2月19日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
87

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
1 Month(s) 至 23 Month(s)(—)
性别
All

入选标准

  • Age range 6 months till 59 months old
  • no evidence of infection and negative c–reactive protein (CRP)
  • hemoglobin below the WHO stipulated cutoff values to define IDA anemia: hemoglobin <11.0 g/dL, MCV <73 fL and serum ferritin < 12 mg/L.
  • no history of consumption of iron supplements for 4 months ago or history of blood transfusion.

排除标准

  • Children who had any signs of infection (fever, vomiting or diarrhea) on blood collection days,
  • children with anemia rather than IDA e.g. hemolytic anemia or haemoglobinopathy (sickle cell disease, beta thalassemia major)
  • children with chronic diseases or drugs that may affect iron absorption

研究者

发起方
Menoufia faculty of medicine

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