chronic spontaneous urticaria
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients with chronic spontaneous urticaria with clinical diagnosis of traditional Chinese and Western medicine; 2. Aged between 18-65 years, no gender limit; 3. No serious heart, liver, lung, kidney and metabolic diseases; 4. Have not received corticosteroids, non-steroids, antihistamines, immunosuppressants and biological agents recently (within 1 month); 5. Disease duration > 6 weeks; 6. Those who voluntarily participate in this experiment, can obey the treatment plan, and sign the informed consent.
Exclusion criteria
Exclusion criteria: 1. Those who have infectious skin diseases, or who have infection, ulcers or scars on the skin of the treatment site; 2. Pregnancy and lactation patients; 3. Patients with malignant tumor, or spontaneous bleeding tendency such as thrombocytopenia and hemophilia; 4. Patients with serious primary diseases such as cerebrovascular, autoimmune diseases or hematopoietic system, mental patients or combined with secondary infection; 5. Patients with severe acute exacerbation of chronic urticaria, such as chest tightness, wheezing, dyspnea involving the laryngeal mucosa, and life-threatening suffocation due to laryngeal edema; those with systemic symptoms such as high fever, chills, and rapid pulse; 6. Those who are participating in other clinical trials or who have participated in other clinical trials within 12 weeks; 7. Patients who are not suitable for inclusion in the group according to the judgment of the doctor.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| measles activity score;chronic urticaria quality of life questionnaire; | — |
Secondary
| Measure | Time frame |
|---|---|
| urticaria control test, UCT;number of wheal episodes;degree of itching; | — |
Countries
China
Contacts
Affiliated Jiangmen Traditional Chinese Medicine Hospital of Ji'nan University