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Clinical Trials/JPRN-UMIN000011241
JPRN-UMIN000011241
Completed
未知

The effects of budesonide/formoterol maintenance and reliever therapy on airway inflammation in asthma patients; open label, randomized parallel group comparison study with fluticasone/salmeterol - The effects of SMART on airway inflammation in asthma patients

Hiroshima Allergy and Respiratory Clinic0 sites30 target enrollmentJuly 21, 2013

Overview

Phase
未知
Intervention
Not specified
Conditions
Bronchial asthma
Sponsor
Hiroshima Allergy and Respiratory Clinic
Enrollment
30
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 21, 2013
End Date
June 30, 2013
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Hiroshima Allergy and Respiratory Clinic

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • \-Patients with a history of hypersensitivity (including contact dermatitis) to any ingredient contained in the study drugs \-Patients with infections with no available effective antimicrobial drugs or with deep seated mycosis \-Patients with tuberculosis \-Patients with rhinitis needed to be treated clinically \-Respiratory infection, judged by the investigator as an infection affecting the asthma, within 8 weeks prior to enrollment \-Use of any beta\-blocking agents (including eye\-drops) \-Treatment with oral, parenteral or rectal steroids within 30 days prior to enrollment \-Any significant disease or disorder judged by the investigator \-Current or previous with a smoking history,10 pack years or more, or smoking cessation no longer than 6 months prior to enrollment \-Pregnancy, breast\-feeding or planned pregnancy during the study \-Suspected poor capability, as judged by the investigator

Outcomes

Primary Outcomes

Not specified

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