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Efficacy of Pranlukast in subjects with Japanese Cedar pollinosis in the OHIO Chamber

Phase 4
Conditions
Japanese cedar pollinosis
Registration Number
JPRN-UMIN000001282
Lead Sponsor
TOPIC Study (Trial of OHIO Chamber-Pranlukast Inhibitory Effect for Cedar Exposure-)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
36
Inclusion Criteria

Not provided

Exclusion Criteria

1) Subjects with a polyp or deformity of the nose. 2) Subjects who used steroid drugs for injection within 6 months before the start of this study. 3) Subjects with systemic diseases ( asthma or tuberculosis ). 4) Subjects with build-up phase of immunotherapy to Japanese cedar pollen. 5) Subjects with pregnancy, lactation or potential pregnancy. 6) Subjects who are inappropriate to this study by the judgment of doctor.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
nose and eye symptoms
Secondary Outcome Measures
NameTimeMethod
the number of sneezing, the amount of nasal secretion, the manifestation time of nasal symptoms, nasal airway resistance, respiratory function and performance test( D-CAT )
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