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Efficacy of Bepotastine besilate OD tablets for Japanese cedar and cypress pollinosis in an artificial exposure chamber(OHIO Chamber)

Efficacy of Bepotastine besilate OD tablets for Japanese cedar and cypress pollinosis in an artificial exposure chamber(OHIO Chamber) - Efficacy of Bepotastine besilate OD tablets for Japanese cedar and cypress pollinosis in an artificial exposure chamber(OHIO Chamber)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000005659
Enrollment
28
Registered
2011-05-30
Start date
2011-06-01
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 and cypress pollinosis

Interventions

Bepotastine besilate OD tablets administered to 14 subjects at twice daily the day before Japanese cedar pollen exposure. The next day(day of Japanese cedar pollen exposure) also administered twice d

Sponsors

Nippon Medical School
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) CAP-RAST score against Japanese cedar pollen and cypress pollen over 2 within the last 3 years. 2) Patients who have typical seasonal allergic rhinitis symptoms for at least 2 years. 3) Patients who are considered eligible medical examination results investigator doctors. 4) Written informed consent is required.

Exclusion criteria

Exclusion criteria: 1) Some patients with mucosal lesion of the nose and eyes. 2) Patients with severe perennial allergic rhinitis or requiring treatment. 3) Patients who received steroid injections within 6 months. 4) Patients with respiratory disease such as asthma. 5) Patients with past history of anaphylaxis. 6) Patients who have the hypersensitivity to study drug. 7) Pregnancy, breast-feeding woman, potential pregnancy, patients who wish to become pregnant during this study. 8) Patients who were judged to be unsuitabele for patinet enrollment by their doctor(Patients who have undergone nasal operation or patients who have undergone immunotherapy).

Design outcomes

Primary

MeasureTime frame
Symptoms score(Nasal, Ocular, Oropharyngeal)

Secondary

MeasureTime frame
1) Occurrence time of the first nasal symptom or the first ocular symptom 2) Nasal secretion volume 3) No of sneezing 4) Digit cancellation test

Countries

Japan

Contacts

Public ContactKiyochika Suematsu

Medical Corporation Shinanokai, Samoncho Clinic Pharmaceutical Dept.,

ki-suematsu@samoncho-clinic.jp+81-3-5366-3641

Outcome results

None listed

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