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Evaluation of the efficacy of Symbicort turbuhaler that target patients with bronchial ashtma complicated by COPD and bronchial asthma - Evaluation of diurnal variation in peak flow -

Evaluation of the efficacy of Symbicort turbuhaler that target patients with bronchial ashtma complicated by COPD and bronchial asthma - Evaluation of diurnal variation in peak flow - - Evaluation of the efficacy of Symbicort turbuhaler that target patients with bronchial ashtma complicated by COPD and bronchial asthma - Evaluation of diurnal variation in peak flow -

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000007708
Enrollment
100
Registered
2012-04-10
Start date
2011-01-01
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

bronchial asthma complicated by COPD and bronchial ashtma

Interventions

symbicort turbuhaler for 2years twice daily, 1-4 inhalation

Sponsors

Department of respirology, graduate School of Medicine, Chiba University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: >COPD (complicated by asthma) or asthma (unquestioned stage) >patients who have inspiratory flow rate can be inhaled test drug >patients who voluntary consent document was obtained after receiving a full explanation upon participation in this study and full understanding >outpatients

Exclusion criteria

Exclusion criteria: >patient wiht an infection refractory to any antibiotics, or deep-seated mycoses >hitory of hypersensitivity to test drug

Design outcomes

Primary

MeasureTime frame
Diurnal variation in PEF by Piko-1

Secondary

MeasureTime frame
expiratory NO eosinophil in sputum serum substance P FEV1.0 FEV1.0 in five minites after inhalaton of Symbicort or Procaterol Hydrochloride chest CT assessment of safty

Countries

Japan

Contacts

Public ContactKen Iesato

Graduate School of Medicine, Chiba University Department of respirology

iesato@gmail.com043-222-7171

Outcome results

None listed

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