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临床试验/ITMCTR2200005651
ITMCTR2200005651尚未招募4 期

Clinical study of snake antipruritic pills in the treatment of chronic spontaneous urticaria

guangdong Provincial Hospital of Chinese Medicine0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
尚未招募
发起方

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
18 至 65(—)
性别
All

入选标准

  • 1. Meet the criteria for diagnosis of chronic spontaneous urticaria: spontaneous wind mass and/or angioedema onset > 6 weeks (Chinese urticaria diagnosis and treatment guide 2018); 2. Age: 18-65 years old, gender-neutral; The degree of itching is light to medium level: light grade is itchy, not obvious (1 point); The number of wind groups is light and medium: light is the number of wind groups< 20 /24h (1 point); Agree to participate in this clinical trial and sign an informed consent form.

排除标准

  • 1. Induced urticaria patients (physical: artificial urticaria (skin scratch), cold-contact urticaria, delayed pressure urticaria, hot-contact urticaria, solar urticaria, vibrating angioedema, choline-energy urticaria; nonphysical: water-source urticaria, contact urticaria); 2. Patients with other diseases that can cause itching; Patients with other life-threatening severe systemic symptoms such as co-infection and throat edema; Combined with serious cardiovascular, liver, kidney and other important organs of internal medicine diseases; 5. Communication barriers, people with mental and mental illness; People who have received glucocorticoids, immunosuppressants, etc. within 3 months; 1 month has used Chinese medicine, acupuncture and other treatment of urticaria; 8. Those who have taken quinoa, pentaphospharide, soap or its preparations within 1 month; Those who have a history of allergies to the active ingredients or preparation aids of the ooselta, or have a history of allergies to other foods or drugs; Patients with pregnancy, lactation or recent birth plans; Need high-altitude operators; 12. Participants in clinical trials of other medical facilities or drugs within 3 months; The researchers did not consider it appropriate for participants.

研究者

发起方
guangdong Provincial Hospital of Chinese Medicine

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