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
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