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Pricking blood therapy for chronic urticaria: a randomized controlled trial

Phase 1
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
Inclusion Criteria

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.

Exclusion Criteria

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
NameTimeMethod
rticaria activity score (UAS);
Secondary Outcome Measures
NameTimeMethod
Visual analogue scale (VAS);Dermatology Life Quality Index (DLQI);
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