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Clinical Observation of Acupoint Application Therapy with Wenfei Tongbi Formula for Patients with Seasonal Allergic Rhinitis in Winter

Clinical Observation on the Treatment of Patients with Seasonal Allergic Rhinitis in Winter Using Acupoint Patching of Wenfei Tongbi Fang

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000882
Enrollment
Unknown
Registered
2026-04-03
Start date
2026-01-16
Completion date
Unknown
Last updated
2026-04-28

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

Conditions

Allergic Rhinitis

Interventions

Control Group:Mometasone nasal spray
Experimental Group:Mometasone nasal spray + acupoint patching

Sponsors

South China University of Integrated Chinese and Western Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) Meets the diagnostic criteria for allergic rhinitis 2) Aged between 18 and 65 years 3) Voluntarily agrees to participate in this trial and is able to adhere to the treatment and observation for 2 weeks 4) No use of medications related to nasal diseases within the past 2 weeks prior to the start of this trial.

Exclusion criteria

Exclusion criteria: 1. Patients with other respiratory system diseases; 2. Patients with severe diseases of the heart, brain, liver, kidney, or hematopoietic system requiring long-term medication; 3. Patients who have used glucocorticoids or immunosuppressive agents within the past month; 4. Patients who are intolerant to the treatment used in this study; 5. Pregnant or breastfeeding women; 6. Patients with allergic reactions to the traditional Chinese medicine or adhesive used in this trial, or those with eczema, dermatitis, or other skin diseases; 7. Patients with severe mental illness who are unable to provide a detailed and complete description of their condition or lack full capacity for independent action; 8. Patients with acute or chronic infectious diseases.

Design outcomes

Primary

MeasureTime frame
Nasal Symptom Total Integral Score Table Total Nasal Symptom Score;

Secondary

MeasureTime frame
Quality of Life Assessment;Serum IgE level;Comprehensive Efficacy Evaluation;

Countries

China

Contacts

Public ContactChen Jing

South China University of Integrated Chinese and Western Medicine Hospital

liuchengjing@126.com13556053733

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: May 1, 2026