Efficacy evaluation of Tiotropium Respimat with AeroChamber Plus
Not Applicable
- Conditions
- COPD
- Registration Number
- JPRN-UMIN000013980
- Lead Sponsor
- Hamamatsu medical center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
1. Known severe allergy to any drugs. 2. Patients with benign prostatic hypertrophy or glaucoma. 3. Patients who cannot parchase AeroChamber Plus. 4. Patients who cannot use tiotropium respimat with inhalation assistance.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change of forced expiratory volume in 1 second (FEV1) after inhalation therapy
- Secondary Outcome Measures
Name Time Method