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Clinical Study on Treatment of Allergic Rhinitis with Lung spleen-deficiencyby improved Xiaochuan Plaster treating Winter Diseases in Summer

Clinical Study on Treatment of Allergic Rhinitis with Lung spleen-deficiencyby improved Xiaochuan Plaster treating Winter Diseases in Summer

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071338
Enrollment
Unknown
Registered
2023-05-11
Start date
2023-06-01
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

allergic rhinitis

Interventions

Test group:Half dose asthma cream + simulant
Control group:Asthmatic: 6 g of asthmatic

Sponsors

Guang'anmen Hospital of China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for moderate to severe Artemisia pollen allergic rhinitis; 2. Comply with the standard of TCM syndrome differentiation of spleen and lung qi deficiency; 3. The age is between 18-60 years old, and the gender is not limited; 4. The course of the disease is more than 1 year; 5. Comply with GCP regulations, sign informed consent, and voluntarily test.

Exclusion criteria

Exclusion criteria: 1) Severe nasal congestion, vasomotor rhinitis, drug-induced rhinitis, other non-allergic rhinitis, respiratory tract Patients with infection, obstructive nasal polyps, or recent upper airway surgery. 2) Fever >38?, or accompanied by other acute infections. 3) Use other Chinese and Western medicines for allergic rhinitis before entering the trial, as follows: use within 1 month Systemic or topical corticosteroids; cromoglycate within 2 weeks; decongestants within 3 days; within 10 days Use loratadine; use ciprofloxacin within 12 weeks; use other drugs that affect nasal symptoms within 3 days. 4) Those under the age of 18 or over 60, or those who are pregnant or breastfeeding. 5) Severe primary cardiovascular disease, liver disease, kidney disease, hematological disease, asthma and other lung diseases disease, or a serious disease that affects their survival, such as cancer or AIDS. 6) Legally or mentally disabled patients. 7) Lost to follow-up due to various reasons. 8) Patients with other immune system diseases and long-term medication.

Design outcomes

Primary

MeasureTime frame
VAS rating;4 nasal symptoms (sneezing, runny nose, itching, and stuffiness);2 eye symptoms (itching/foreign body sensation/redness, tears);

Secondary

MeasureTime frame
rhinoconjunctivitis quality of life questionnaire, RQLQ;Psychological state score;Cellular inflammatory factors;

Countries

China

Contacts

Public ContactZhang Yu

Guang'anmen Hospital of China Academy of Chinese Medical Sciences

gam2739@aliyun.com+86 136 4126 6098

Outcome results

None listed

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