Efficasy of assist usage of inhaled procaterol on improving dyspnea symptom and QOL in daily activities of patients with COPD
Not Applicable
- Conditions
- chronic obstructive pulmonary disease
- Registration Number
- JPRN-UMIN000002800
- Lead Sponsor
- Dept. of Allergy and Respiratory Medicine, Tohno-Kousei Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Not provided
Exclusion Criteria
1) present smokers and ex-smokers within 1 year, 2) treatment with other SABAs in the previous 3 months, 3) treatment with oral or intravenous corticosteroids in the previous 3 months, 4) new induction of home oxygen therapy (HOT) in the previous 6 months, 5) other chronic respiratory disease, 6) taking medication for chronic respiratory infectious diseases, 7) severe hepatic, heart or renal disease, hematologic diseases or other grave complications, 8) history of poor drug compliance, and 9) inappropriate from the doctor's perspective.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method dyspnea symptom score QOLs
- Secondary Outcome Measures
Name Time Method pulmonary function tests impulse oscillometry system (IOS)