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Multicentric study of combination therapy of theophylline and tiotropium in COPD

Not Applicable
Conditions
Chronic obstructive pulmonary disease (COPD)
Registration Number
JPRN-C000000367
Lead Sponsor
Graduate school of biomedical sciences, Hiroshima university, department of molecular and internal medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
100
Inclusion Criteria

Not provided

Exclusion Criteria

Patients for whom theophylline or tiotropium is contraindicated Patients who have used other long acting bronchodilator, other xanthine, and inhaled corticosteroid within 1 month Patients with asthma Patients who need persistant oxygen therapy Patients with respiratory infection within 1 month Patients with severe hepatic, renal, heart, hematologic abnormality Patients with active tuberculosis or pulmonary sequelae of tuberculosis Patients with cancer within 2 years. (excluding basal cell carcinoma) Patients with cystic fibrosis and bronchiectasis Patients who are or could be pregnant In addition to the above exclusion criteria, patients judged to be inadequate to participate in this study by their physician

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ung function test QOL (St George Respiratory Questionnaire)
Secondary Outcome Measures
NameTimeMethod
Blood concentration of theophylline Induced sputum
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