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The additive effects of Pranlukast in stable asthmatic patients with the regular use of FP/LABA combination drug –(1) Open-label, randomized and comparative study–

The additive effects of Pranlukast in stable asthmatic patients with the regular use of FP/LABA combination drug –(1) Open-label, randomized and comparative study– - The additive effects of Pranlukast in stable asthmatic patients with the regular use of FP/LABA combination drug –(1) Open-label, randomized and comparative study–

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000001006
Enrollment
50
Registered
2008-02-04
Start date
2008-03-01
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

Asthma

Interventions

Treatments with FP/LABA combination drug and Pranlukast for 4 weeks. Treatments with FP/LABA combination drug for 4 weeks.

Sponsors

JA Tohno Kousei Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients with FP/LABA combination drug more than 3 months 2.Stable asthmatic patients who evaluate themselves to be well-controlled or better

Exclusion criteria

Exclusion criteria: 1.Past treatments with anti-LT drugs in the previous 3 months. 2.Past treatments with oral corticosteroids in the previous 2 weeks. 3.Chronic obstructive lung disease (COPD) and other respitatory disease. 4.Severe liver, kidney, heart , hematic and other diseases 5.Inappropriate patients from the doctor's viewpoint.

Design outcomes

Primary

MeasureTime frame
Peripheral airway inflammation in induced sputum (Eosinophils and ECP)

Secondary

MeasureTime frame
1.Asthmatic symptoms and QOL(AQLQ) 2.Pulmonary functions (PEF, FEV1, FEF50,FEF75) 3.Eosinophils in peripheral blood

Countries

Japan

Contacts

Public ContactHiroyuki Ohbayashi

JA Tohno Kousei Hospital Allergy and respiratory Medicine

ohbayasi@nn.iij4u.or.jp0572-68-4111

Outcome results

None listed

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