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Clinical Study on the Treatment of Cough Variant Asthma (Wind Cold Invading Lung Syndrome) with Shufeng Zhike Formula

Clinical Study on the Treatment of Cough Variant Asthma (Wind Cold Invading Lung Syndrome) with Shufeng Zhike Formula

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097686
Enrollment
Unknown
Registered
2025-02-24
Start date
2024-03-01
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Cough Variant Asthma

Interventions

Control Group:Budesonide and Formoterol Fumarate Powder for Inhalation(160ug:4.5ug*60take),one puff each time, twice a day, without Chinese medicine.
Intervention Group:Budesonide and Formoterol Fumarate Powder for Inhalation(160ug:4.5ug*60take),one puff each time, twice a day + Shufengzhike fomula,one packet each time, twice a day.

Sponsors

Guangzhou Panyu Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Meet the western medical diagnostic criteria for CVA and the Chinese medicine diagnosis is wind-cold against the lungs; (2) Patients aged 18-80 years (inclusive); (3) Voluntarily participate and sign an informed consent form after fully understanding the treatment plan of this experiment; (4) If they have other diseases at the same time, but the consultation period does not affect this study and does not require special treatment; Patients who fulfill all the above conditions will be included as cases.

Exclusion criteria

Exclusion criteria: (1) Those with confirmed diagnosis of other chronic respiratory diseases, such as chronic bronchitis and interstitial pulmonary fibrosis; (2) Patients with missing medical record information; (3) Patients with a previous history of chronic heart failure, hepatic and renal insufficiency, and other combinations of more serious primary diseases of other systems; (4) Pregnant and lactating patients; (5) Patients who are intolerant or allergic to the study drug; (6) Subjects with poor compliance, using therapies other than the study or changing therapies on their own during the treatment period; Subjects meeting any of the above were excluded.

Design outcomes

Primary

MeasureTime frame
Effective rate;

Secondary

MeasureTime frame
Visual Analogue Scale;Cough Evaluation Test;Cough relief time and Cough disappearance time;Clinical Syndrome Score of Chinese medicine;Leicester Cough Questionnaire;

Countries

China

Contacts

Public ContactSheng Luo

Guangzhou Panyu Hospital of Chinese Medicine

tcm2007@163.com+86 135 6018 4266

Outcome results

None listed

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