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临床试验/IRCT201107317164N1
IRCT201107317164N1已完成2 期

Comparison of the effects of Oral charcoal capsule with Aluminum Hydroxide Syrup on pruritus in hemodialytic patients in Gorgan 5th – Azar hospital.

Golestan medical Sciences university, Vice chancellor for research0 个研究点目标入组 30 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
发起方
入组人数
30

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
no limit 至 no limit(—)
性别
All

入选标准

  • At least 2 weeks history of Uremic pruritus; Having Moderate or severe pruritus {based on measurement of Pruritus scale (MPS) or Visual Analog Scale (VAS)}; At least 6 months history of hemodialysis; Tree time hemodialysis in week and four hours for each session.
  • exclusion criteria: Having Dermal or non Dermal Causer Pruritus

排除标准

  • 未提供

研究者

发起方
Golestan medical Sciences university, Vice chancellor for research

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