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Clinical Trials/JPRN-UMIN000003492
JPRN-UMIN000003492
Completed
Phase 4

Efficacy and safety of regular treatment with procaterol and budesonide inhalation suspension for young children with moderate persistent asthma. - Budesonide + Procaterol Inhalation Therapy Study (BUPIT study)

niversity of Toyama, Faculty of Medicine, Department of Pediatrics0 sites50 target enrollmentApril 14, 2010

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Bronchial Asthma
Sponsor
niversity of Toyama, Faculty of Medicine, Department of Pediatrics
Enrollment
50
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 14, 2010
End Date
June 1, 2011
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversity of Toyama, Faculty of Medicine, Department of Pediatrics

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\.Patients who have an event listed below within a month a)Respiratory infection disease that required hospitalization b)Administration of systemic corticosteroids 2\.Recieving regular use of inhaled corticosteroids or beta 2 agonists in the previous 3 months 3\.Patients who have severe chronic diseases 4\.Patients who have chronic low airway diseases other than bronchial asthma 5\.Any other children considered by the attending physicians as inappropriate for participation in this study

Outcomes

Primary Outcomes

Not specified

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