跳至主要内容
临床试验/TCTR20220302003
TCTR20220302003招募中3 期

Butyrate supplements improve efficacy in patients with moderate to severe chronic spontaneous urticaria, A randomized, double-blind, placebo-controlled trial

Department of Medicine of Phramongkutklao hospital0 个研究点目标入组 40 人开始时间: 2022年3月2日最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
40

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
20 Years 至 60 Years(—)
性别
All

入选标准

  • chronic urticaria patients who symptoms do not improve with second generation antihistamine drug

排除标准

  • 1. History of butyrate allergy
  • 2. Immunocompromised patient , psychiatric , kidney impairment and hepatic impairment patient
  • 3. Patient need to take other medicine for chronic urticaria treatment other than second generation antihistamine drug eg. H2 antagonists , leukotriene receptor antagonists, first-generation antihistamine, cyclosporine or omalizumab
  • 4. Pregnant

研究者

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