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Research on Effects of Bleeding Therapy on Chronic Idopathic Urticaria and Operational Specifications

Research on Effects of Bleeding Therapy on Chronic Idopathic Urticaria and Operational Specifications

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015294
Enrollment
Unknown
Registered
2018-03-21
Start date
2018-03-31
Completion date
Unknown
Last updated
2018-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Idiopathic Urticaria

Interventions

treatment group: bleeding therapy with cupping and Ebastine tablets
cupping group:cupping and Ebastine tablets
Ebastine group:Ebastine tablets

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. urticaria diagnosed by criteria from EAACI/GA2LEN/EDF/WAO/Urticaria Guidline; 2. score of UAS7 no less than 28; 3. aged between 18~70 years male and female; 4. vollenteers who sign up the informed consent and capable of following physicians' advice.

Exclusion criteria

Exclusion criteria: 1. patient has been taking antihistamine drugs within 3 days, or corticosteroid, non-steroidal anti-inflammatory drugs or immunosuppressive drugs within 1 month; 2. course of urticaria more than 2 years; 3. autoimmune urticaria; 4. severe autoimmune diseases such SLE; 5. allergic to Ebastine; 6. pregnant or lactating women; 7. thrombocytopenia and coagulation dysfunction; 8. abnomal blood routine, liver function or kidney function examination; 9. patients with severe systemic symptoms accompanied by shock, with obvious surgical injuries, specific causes of infection, or high fever, dizziness, headache, and vomiting during visit; 10. combined with severe primary diseases such as cardiovascular diseases, diabetes, bone metabolism abnormalities, liver or kidney diseases, acute stage of asthma or hematopoietic diseases; Others: patients with mental illness; ulcer, infection or scar on the treatment site.

Design outcomes

Primary

MeasureTime frame
Urticaria Activity Score, UAS;

Countries

China

Contacts

Public ContactMa Biru

Guangdong Hospital of Chinese Medicine

71280647@qq.com+86 136789789

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026