ITMCTR2100004975招募中1 期
To Explore the Clinical Efficacy and Mechanism of optimized 'xiao-feng-san'
适应症
试验速览
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional study
入排标准
- 年龄范围
- 20 至 48(—)
- 性别
- All
入选标准
- •1. Patients aged 20 to 48 years;
- •2. patients conforming to the diagnostic criteria of refractory chronic urticaria;
- •3. patients conforming to the diagnostic criteria of TCM wind-heat syndrome;
- •4. patients having used at least 2 times the conventional dose of antihistamines or at least 2 combined antihistamines with conventional dose for more than 2 weeks;
- •5. The duration of patients'hives is more than 2 hours;
- •6. patients able to give stool samples;
- •7. patients able to sign the informed consent form.
排除标准
- •1. Patients dignosed drug-induced urticaria, induced urticaria (cold urticaria, febrile urticaria, cholinergic urticaria), urticaria vasculitis and other skin diseases with urticaria-like manifestations;
- •2. patients who have been treated well with antihistamines or have been treated with hormones, immunosuppressants, or biological agents, or have received relevant Chinese medicine treatment 1 week before enrollment,or Patients who have received antibiotics and non-steroidal anti-inflammatory drugs 2 weeks before enrollment;
- •3. patients who are pregnant, or preparing for pregnant, or breastfeeding women;
- •4. patients suffering serious organic diseases of important organs such as heart, brain, liver and kidney,and those with severe primary diseases of the hematopoietic system, and those with mental illness;
- •5. patients allergic to the components of Chinese medicine in the research prescription.
研究者
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