Bronchial Asthma
Conditions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: For bronchial asthma: 1. Age ranged from 18-65 years old without gender limitation; 2. Patients diagnosed with bronchial asthma according to the "2016 guidelines for the prevention and treatment of bronchial asthma of the Chinese respiratory society" and the "2019GINA". 3. Patients who voluntarily participate in the study and sign the informed consent. For health control: 1. Age ranged from 18-65 years old without gender limitation; 2. Patients diagnosed with no bronchial asthma according to the "2016 guidelines for the prevention and treatment of bronchial asthma of the Chinese respiratory society" and the "2019GINA". 3. Patients who voluntarily participate in the study and sign the informed consent.
Exclusion criteria
Exclusion criteria: For bronchial asthma: 1) Have participated in or are currently participating in other clinical trials within 1 month prior to this study; 2) Use of systemic glucocorticoids within 1 month prior to the study; 3) Systemic infection or respiratory bacterial infection, tuberculosis, fungal infection within 1 month prior to the study; 4) Severe acute asthma attack and hospitalization within the past 3 months prior to the study; 5) Changes in regular asthma treatment during the initial 3 months of the study period; 6) Patients with significant underlying conditions such as hypertension, tumor, cardiovascular disease, liver disease, kidney disease, and hematopoietic disorders; 7) Asthma caused by other diseases such as tuberculosis, bronchiectasis, and cardiac insufficiency; 8) Hyperthyroidism diagnosis; 9) Presence of mental illnesses that impair self-control and accurate expression; 10) Pregnant or lactating women; 11) Other conditions deemed unsuitable for participation in the study by healthcare professionals. The patient's apparent illness raised concerns among researchers regarding potential risks or impact on study results. For health control: 1) Have participated in or are currently participating in other clinical trials within 1 month prior to this study; 2) Use of systemic glucocorticoids within 1 month prior to the study; 3) Systemic infection or respiratory bacterial infection, tuberculosis, fungal infection within 1 month prior to the study; 4) Patients with other allergic conditions, such as allergic rhinitis and allergic dermatitis. 5) Patients with significant underlying conditions such as hypertension, tumor, cardiovascular disease, liver disease, kidney disease, and hematopoietic disorders; 6) Hyperthyroidism diagnosis; 7) Presence of mental illnesses that impair self-control and accurate expression; 8) Pregnant or lactating women; 9) Other conditions deemed unsuitable for participation in the study by healthcare professionals. The patient's apparent illness raised concerns among researchers regarding potential risks or impact on study results.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| lung function;Quality of Life Score;Peripheral blood eosinophil count;Peripheral blood inflammatory cytokines; | — |
Secondary
| Measure | Time frame |
|---|---|
| General clinical data; | — |
Countries
China
Contacts
Shanghai Research Institute of Acupuncture and Meridian,Yueyang Hospital of Integrated Chinese and Western Medicine affiliated to Shanghai University of Traditional Chinese Medicine