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Acupuncture for patients with chronic spontaneous urticaria: A randomized, sham-controlled pilot trial

Phase 2
Completed
Conditions
Chronic Urticaria
Registration Number
ITMCTR2100005452
Lead Sponsor
Chengdu University of Traditional Chinese Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Eligible participants were diagnosed by three specialists in dermatology according to EAACI/GA2LEN/EDF/WAO guidelines for CSU and participants met the following inclusion criteria were included: 1) the sudden appearance of wheals, angioedema, or both; 2) the occurrence of spontaneous wheals, angioedema, or both for = 6 weeks; 3) suffering from urticaria at least twice a week on average during the previous 6 weeks; 4) aged between 18 to 70 years; 5) antihistamines were not used within 2 weeks before entering the study; 6) steroids hormone and immunosuppressive drugs were not used within 1 month; 7) agreed to participate in this study and signed written informed consent.

Exclusion Criteria

Participants meeting any of the following criteria were excluded: 1) urticaria was inducible by physical factors (e.g., cold urticaria, delayed pressure urticaria, solar urticaria, heat urticaria, vibratory angioedema); 2) suffering from neurological diseases, mental disorders, immunodeficiency, bleeding disorders; 3) having any serious disease of the heart, liver, kidney, or other organs; 4) having severe cognitive impairment; 5) pregnant or lactating; 6) involved in other clinical studies at the same time.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
rticaria Activity Score;
Secondary Outcome Measures
NameTimeMethod
Dermatology Life Quality Index;Hamilton Depression Scale;Visual Analogue Scale (VAS) score of itching intensity;Hamilton Anxiety Scale;
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