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

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

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000002390
Enrollment
60
Registered
2009-08-26
Start date
2009-11-01
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

Cough variant asthma

Interventions

Inhale Salmeterol/fluticasone propionate combination 250 mcg twice daily Inhale Fluticasone propionate 200 mcg twice daily, and take Montelukast 10 mg once daily

Sponsors

Kyoto University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Couth variant asthma patients 2)Patients who are still poorly controlled despite monotherapy with inhaled corticosteroids 3)Patients who gave consent to the study

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
Visual analogue scale score of cough

Secondary

MeasureTime frame
1)Parameters of impulse oscillometry 2)Indices of pulmonary function 3)Indices of Capsicine cough sensitivity 4)Exhaled nitric oxide concentrations 5)Biomarker levels of induced sputum 6)Biomarker levels of serum and urine 7)Scores of questionnaires

Countries

Japan

Contacts

Public ContactTomoko Tajiri

Kyoto University Graduate School of Medicine Department of Respiratory Medicine

tomookot@kuhp.kyoto-u.ac.jp075-751-3830

Outcome results

None listed

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