Study on technical specification and curative effect evaluation of warming lung and guyuan umbilical moxibustion for chronic obstructive pulmonary disease
- Conditions
- Chronic obstructive pulmonary disease
- Registration Number
- ITMCTR2100005162
- Lead Sponsor
- The First Affiliated Hospital of Henan University of Chinese Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- Not specified
1. Patients with stable COPD diagnosis;
2. Aged 40 to 80 years;
3. Patients with qi deficiency syndrome (lung qi deficiency, lung spleen deficiency, lung and kidney qi deficiency);
4. The number of acute exacerbations in the previous year >= 1;
5. Not participating in clinical studies of other interventions within 1 month before enrollment;
6. Able to tolerate lung-warming and solid-element umbilical moxibustion therapy;
7. Voluntarily accept the treatment and sign the informed consent.
1. Pregnant and lactating women;
2. Confused, dementia, various mentally ill patients;
3. Combined with severe cardiac insufficiency;
4. Patients with active pulmonary tuberculosis, diffuse panbronchiolitis, pneumothorax, pleural effusion, and pulmonary embolism;
5. Combined with neuromuscular diseases affecting respiratory and motor function;
6. Combined tumor;
7. Severe liver and kidney disease (ALT/AST>=3 times normal value, glomerular filtration rate GFR<=29);
8. Those who are known to be allergic to the composition of moxibustion powder.
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method umber and severity of chronic obstructive pulmonary disease acute exacerbations;
- Secondary Outcome Measures
Name Time Method Quality of life;Evaluation of skin sensitization;Effectiveness satisfaction questionnaire;Clinical symptoms and signs;6 minutes walking distance;Dyspnea classification;Lung function;Patient Reported Outcome;