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Clinical study of pranlukast as early seasonal treatment for Japanese cedar pollinosis

Phase 4
Conditions
Japanese cedar pollinosis
Registration Number
JPRN-UMIN000000583
Lead Sponsor
Group study of Early Intervention of Pollinosis with Pranlukast
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Sex
All
Target Recruitment
200
Inclusion Criteria

Not provided

Exclusion Criteria

1) any other disease, nasal polyp, acute/chronic rhinitis, sinusitis et al 2) use of any anti-histamine drugs, anti-allergy drugs, nasal steroid drugs et al at the beginning of the study 3) buildup phase of immunotherapy to Japanese cedar pollen 4) pregnancy, potential pregnancy, or lactation 5) the others, inappropriate to this study by the judgment of doctor

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Symptom-medication score (symptomscore+medication score)
Secondary Outcome Measures
NameTimeMethod
Symptom score (stuffy nose,runny nose, sneezing,eye itchiness and tearing), medication score and QOL Questionaire score(JRQLQ No1)
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