A prospective observational study of switching to single-inhaler triple combinations in patients with obstructive pulmonary disease
Not Applicable
- Conditions
- Chronic obstructive pulmonary disease and bronchial asthma
- Registration Number
- JPRN-UMIN000043389
- Lead Sponsor
- Shizuoka General Hospital, respiratory medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Not provided
Exclusion Criteria
1. Patients with airway infection within 3 months 2. Patients who are contraindicative for single-inhaler triple therapy
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method A change of FEV1 after 8 weeks
- Secondary Outcome Measures
Name Time Method A change of symptom score, FVC, IC, respiratory impedance, FeNO after 8 weeks