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Efficacy of Aerobika

Phase 4
Conditions
Chronic Obstructive Pulmonary Disease
COPD
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
Inclusion Criteria

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.

Exclusion Criteria

The condition that the investigator judges to exclude from the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in FEV1 before and after 4-week treatment with Aerobika.
Secondary Outcome Measures
NameTimeMethod
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
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