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Clinical Efficacy of the "San Qi Yun Zhen" Acupuncture Technique for Chronic Urticaria and Its Mechanism in Inhibiting FceRI-IgE Cross-linking

Clinical Efficacy of the "San Qi Yun Zhen" Acupuncture Technique for Chronic Urticaria and Its Mechanism in Inhibiting FceRI-IgE Cross-linking

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000599
Enrollment
Unknown
Registered
2026-03-18
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Urticaria

Interventions

Acupuncture group:acupuncture treatment

Sponsors

Shanghai Research Institute of Acupuncture and Meridian
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Meets the diagnostic criteria for Chronic Urticaria (CU) according to both Traditional Chinese Medicine (TCM) and Western Medicine, and is currently in the active flare-up phase. Aged between 20 and 65 years (inclusive), regardless of gender. Demonstrates full understanding of the study, agrees to participate, and provides a signed Informed Consent Form (ICF).

Exclusion criteria

Exclusion criteria: Inducible urticaria (e.g., physical, cholinergic, aquagenic, or contact urticaria), urticaria with a clearly identifiable etiology (e.g., drug-induced or infection-related), and urticarial vasculitis. Patients with a prior history of acupuncture treatment. Use of antihistamines (e.g., ebastine, cetirizine, diphenhydramine, chlorpheniramine, promethazine, ketotifen, loratadine), glucocorticoids, or immunosuppressants within the past month. Women who are pregnant or breastfeeding. Individuals with contraindications to acupuncture, such as hemorrhagic diseases, a history of fainting during acupuncture (needle syncope), or local skin infections, ulcers, scar tissue, and tumors. Patients with psychiatric disorders or other severe systemic diseases (e.g., serious cardiac, hepatic, or renal impairment). Other patients who do not meet the inclusion criteria.

Design outcomes

Primary

MeasureTime frame
Clinical symptom score;

Secondary

MeasureTime frame
Dermatology Life Quality Index;Urticaria Control Test;Serum Immunoglobulin E;Fc epsilon receptor I alpha chain (FceRIa );Linker for activation of T cells (LAT);Spleen Tyrosine Kinase(SYK);Phosphorylated Phosphatidylinositol 3-kinase(p-PI3K);ß-N-Acetylhexosaminidase (ß-Hex);

Countries

China

Contacts

Public ContactXin Zhang

Shanghai Research Institute of Acupuncture and Meridian

tiancaiani@qq.com13816991324

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Apr 4, 2026