Pricking blood therapy for chronic urticaria: a randomized controlled trial
- Conditions
- Chronic Urticaria
- Registration Number
- ITMCTR2100005233
- Lead Sponsor
- Hebei University of Chinese Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- Not specified
1. Those who meet the diagnostic criteria of chronic urticaria in the EAACI/GA2LEN/EDF/WAO guidelines for the treatment of urticaria (2017) and the Chinese guidelines for the treatment of urticaria (2018);
2. Aged 18-70 years;
3. No antihistamines use within 2 weeks before enrollment and no steroids or immunosuppressive drugs within 1 month;
4. The liver and kidney functions are normal;
5. Not participating in other ongoing clinical studies;
6. Voluntary participation and signed informed consent form.
1. Unconscious people who cannot express subjective symptoms of discomfort and psychiatric patients;
2. Those with Progressive malignant tumors or other serious wasting diseases, who are prone to co-infection and bleeding;
3. Patients with severe primary diseases such as cardiovascular, liver, kidney, digestion, hematopoietic system;
4. Pregnant and lactating women.
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method rticaria activity score (UAS);
- Secondary Outcome Measures
Name Time Method Visual analogue scale (VAS);Dermatology Life Quality Index (DLQI);