A comparative study on the curative effect of acupoint application on patients in remission of allergic asthma which based on the lung-gut axis theory
- Conditions
- asthma
- Registration Number
- ITMCTR2100004320
- Lead Sponsor
- The First Affiliated Hospital of Zhejiang Chinese Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- Not specified
(1) Cases that are clearly diagnosed according to the diagnostic criteria of western medicine for asthma and are in the acute stage of non-asthma;
(2) Remission period of asthma in accordance with TCM syndrome differentiation standards;
(3) Do not use other immune enhancers, do not inhale glucocorticoids or other drugs or short-term inhalation of glucocorticoids (less than 1 month per year) during the treatment;
(4) Aged from 18 to 65 years;
(5) Those who sign an informed consent and are willing to follow the research plan.
(1) Patients with other diseases that can cause asthma or breathing difficulties;
(2) Pregnant and lactating women who are allergic to the prescription drugs in this trial;
(3) Those who suffer from heart failure, moderate to severe hypertension, diabetes, and other blood system diseases or mental illnesses who cannot cooperate;
(4) People with scar constitution or history of tape allergy, or unhealed wounds exposed in acupoint application;
(5) Other diseases that are not suitable for acupoint application.
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Clinical efficacy score;Self-rating anxiety scale;Depression self-rating scale score;Adult asthma quality of life score;
- Secondary Outcome Measures
Name Time Method Serum related immune index;