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Multicentric study of combination therapy of theophylline and tiotropium in COPD

Multicentric study of combination therapy of theophylline and tiotropium in COPD - Theophylline and tiotropium in COPD

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-C000000367
Enrollment
100
Registered
2006-04-01
Start date
2006-01-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic obstructive pulmonary disease (COPD)

Interventions

After 4 weeks of administration of tiotropium, both oral theophylline(200-800mg/day) and tiotropium will be administerd for 4 weeks.

Sponsors

Graduate school of biomedical sciences, Hiroshima university, department of molecular and internal medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: COPD patient with a persistant symptoms(chronic cough, sputum, dyspnea), 45 years old or older, Post bronchodilator FEV1/FVC<70%, Smoking history 10 pack-years or more Patients who have signed the agreement for participation in this study

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
Lung function test QOL (St George Respiratory Questionnaire)

Secondary

MeasureTime frame
Blood concentration of theophylline Induced sputum

Countries

Japan

Contacts

Public ContactYoshinori Haruta

Graduate school of biomedical sciences, Hiroshima university Department of molecular and internal medicine

082-257-5196

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026