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A comparison of regular and as-needed use of Mometasone furoate hydrate nasal spray in the treatment of Japanese cedar pollinosis

A comparison of regular and as-needed use of Mometasone furoate hydrate nasal spray in the treatment of Japanese cedar pollinosis - Mometasone furoate hydrate nasal spray for pollinosis: regular versus as-needed use

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000001644
Enrollment
100
Registered
2009-01-17
Start date
2009-01-01
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

Japanese cedar pollinosis

Interventions

Regular use group: Taking two puffs of Mometasone furoate hydrate nasal spray into each nostril (total 200 ug/day) every morning from the onset of nasal symptoms. As-needed use group: Taking two puffs

Sponsors

Department of Otorhinolaryngology, Head & Neck Surgery, Faculty of Medicine, University of Yamanashi
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) A history of Japanese cedar pollinosis for at least one season before study entry. 2) Positive allergy skin test to Japanese cedar pollen or Japanese cedar pollen specific IgE RAST score >= class 2. 3) Written informed consent is required.

Exclusion criteria

Exclusion criteria: 1) Taking any immunosuppressive drugs or systemic steroid drugs within six months before study entry. 2) Taking any antibiotics within two weeks before study entry. 3) Taking any anti-allergy drugs within two weeks before study entry. 4) Using any anti-allergy nasal drops within two weeks before study entry. 5) Under treatment of buildup phase of specific immunotherapy. 6) Patients with deflected nasal septum, sinusitis, or nasal polyps which cause a barrier to evaluate nasal symptoms. 7) Patients with upper respiratory inflammation, respiratory infection, or severe bronchial asthma. 8) Patients with severe cardiac, hepatic, kidney, or hematological disease. 9) A history of hypersensitivity to mometasone furoate hydrate, loratadine, or sodium cromoglycate. 10) Pregnant or lactating women and women who may be pregnant. 11) Taking a drug of erythromycin or cimetidine.

Design outcomes

Primary

MeasureTime frame
Overall quality of life score of Rhinoconjunctivitis Quality of Life Questionnire.

Secondary

MeasureTime frame
1) Each score of seven domains of RQLQ. 2) Two summary scores (PCS and MCS) of SF-36 v2. 3) Each severity score of four daily nasal symptoms (runny nose, itchy nose , stuffy nose, and sneezing). 4) Total nasal symptom score (the sum of four nasal symptom scores). 5) Each severity score of three daily ocular symptoms (eye itchiness, eye redness, and tearing). 6) Total ocular symptom score (the sum of three ocular symptom scores).

Countries

Japan

Contacts

Public ContactGoro Takahashi

University of Yamanashi Department of Otorhinolaryngology, Head & Neck Surgery

tgoro@yamanashi.ac.jp055-273-6769

Outcome results

None listed

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