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
Not Applicable
Recruiting
- Conditions
- bronchial asthma complicated by COPD and bronchial ashtma
- Registration Number
- JPRN-UMIN000007708
- Lead Sponsor
- Department of respirology, graduate School of Medicine, Chiba University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
>patient wiht an infection refractory to any antibiotics, or deep-seated mycoses >hitory of hypersensitivity to test drug
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Diurnal variation in PEF by Piko-1
- Secondary Outcome Measures
Name Time Method 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