Skip to content

Clinical Efficacy of Lue Biyan Formula in The Treatment of Lung Qi Deficiency and Cold Type Allergic Rhinitis and Its Influence on Th1/Th2 and Th17/Treg Balance

Clinical Efficacy of Lue Biyan Formula in The Treatment of Lung Qi Deficiency and Cold Type Allergic Rhinitis and Its Influence on Th1/Th2 and Th17/Treg Balance

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000597
Enrollment
Unknown
Registered
2025-03-26
Start date
2023-11-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Allergic rhinitis

Interventions

Sponsors

China-Japan Friendship Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Age>18 years old and<60 years old; 2. Meet the diagnostic criteria of AR Western medicine; Severe or severe symptoms that have a significant impact on quality of life with symptoms occurring for more than 4 days per week and for = 4 consecutive weeks; The patient has at least three nasal symptoms (1) sneezing 2) watery nasal discharge 3) nasal itching 4) nasal congestion) and the daily average VAS score for each symptom is = 5 points; Or if there are 2 or more nasal symptoms (itching sneezing watery nose and nasal congestion) and at least one symptom scores = 2 points (on a four point scale); 3. Meet the traditional Chinese medicine syndrome differentiation criteria for nasal and lung qi deficiency and cold; 4. No history of asthma attacks or other allergic diseases within 3 months prior to enrollment; No use of glucocorticoids or antihistamines or leukotrienes within the week prior to enrollment; 5. Those who voluntarily sign the informed consent form; 6. Patients who have not participated in AR clinical research in the past 3 months;

Exclusion criteria

Exclusion criteria: 1. Patients with combined rheumatic and autoimmune diseases; 2. Patients with nasal organic lesions such as sinusitis and nasal polyps bronchial asthma or other serious pulmonary complications; 3. Patients with combined tumors or severe impairment of heart liver kidney and other functions; 4. Those who are unable to cooperate due to mental illness or other reasons; 5. Pregnant or lactating individuals or those who have the ability to conceive and are unwilling/unable to take effective contraceptive measures; 6. History of smoking or drug abuse; 7. Those who have used local or systemic corticosteroids or other immunosuppressants in the past 3 months; 8. Those who have used mast cell membrane stabilizers anticholinergic drugs decongestants in the past week and those who have used local or systemic corticosteroids or other immunosuppressants in the past 3 months; 9. Those who have used antihistamines and leukotrienes in the past week; 10. Those who have undergone nasal surgery within the past week; 11. Individuals with a history of allergies to the ingredients of the experimental drug.

Design outcomes

Primary

MeasureTime frame
Clinical symptom scoring;

Secondary

MeasureTime frame
Allergen Total IgE;Traditional Chinese Medicine Syndrome Score for Lung Qi Deficiency and Cold Syndrome;cytokine;Peripheral blood eosinophil count;

Countries

China

Contacts

Public ContactJia Mingyue

China-Japan Friendship Hospital

mingyue131415@163.com15210723090

Outcome results

None listed

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