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临床试验/IRCT138710291562N1
IRCT138710291562N1已完成2 期

Evaluating the Effect of Cromolyn Sodium in Uremic Pruritus

Shiraz University of medical sciences0 个研究点目标入组 60 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
60

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

  • Inclusion Criteria:
  • Hemodialysis patients > 18 yo suffering from pruritus for at least 6 weeks, and who have not responded to other drugs
  • Willing and able to give informed concent

排除标准

  • Known dermatologic, liver, metabolic disease, or any other disease or condition other than ESRD that causes pruritus
  • consumption of antihistamines or other antipruritic drugs
  • Lactase deficiency

研究者

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