Efficacy of Aerobika
- Conditions
- Chronic Obstructive Pulmonary DiseaseCOPD
- Registration Number
- JPRN-jRCT1032180010
- Lead Sponsor
- Mineshita Masamichi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 30
Subject has post-long acting bronchodilator forced expiratory volume in first second (FEV1) is less than 80% predicted.
Subject has declared that he/she has stopped smoking for at least 8 weeks prior to entering the study.
Subject has respiratory symptoms 10 and over on the CAT total score, and has the phlegm symptoms 2 and over on the CAT phlegm score.
Subject has read, understood, and signed the informed consent form.
The condition that the investigator judges to exclude from the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change in FEV1 before and after 4-week treatment with Aerobika.
- Secondary Outcome Measures
Name Time Method Following parameters will be assessed for before and at 4-week treatment with Aerobika.<br>1. VC, FVC, V50, and V25<br>2. IOS (R5, R5ins, R5exp, R20, X5, X5ins, X5exp, Fres, Ax)<br>3. 6 minute-walking test<br>4. CAT score, mMRC<br>5. Acute exacerbation