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Clinical Trials/JPRN-UMIN000002390
JPRN-UMIN000002390
Completed
Phase 4

Study to examine the effects of Salmeterol/fluticasone propionate combination(SFC) in patients with cough variant asthma(CVA) - Study to examine the effects of SFC in CVA

Kyoto University Graduate School of Medicine0 sites60 target enrollmentAugust 26, 2009

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Kyoto University Graduate School of Medicine
Enrollment
60
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 26, 2009
End Date
March 1, 2014
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Kyoto University Graduate School of Medicine

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\)Patients without cough symptom in the last 1 week before enrollment 2\)Patients with other respiratory diseases 3\)Patients taking Long acting be\-ta 2 agonist(LABA) or Leukotriene receptor antagonist(LTRA) 4\)Patients who are given systemic corticosteroid in the last 4 weeks 5\)Patients who suffered from upper respiratory infection in the last 4 weeks 6\)Patients who had smoked in the last 6 months, or who had smoked more than 10 pack year in the past 7\)Patients who are considered inappropriate by physicians in charge

Outcomes

Primary Outcomes

Not specified

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