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Investigation of patient satisfaction to Second-generation antihistamines in the treatment of Japanese cedar and cypress family pollinosis.

Investigation of patient satisfaction to Second-generation antihistamines in the treatment of Japanese cedar and cypress family pollinosis. - Investigation of patient satisfaction in pollinosis to antihistamines.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000003132
Enrollment
300
Registered
2010-02-03
Start date
2010-02-01
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 family pollinosis

Interventions

From the first medical examination, administer 5 mg as olopatadine hydrochloride twice a day orally in the morning and at bedtime , at least two weeks. From the first medical examination, administe

Sponsors

Department of Otorhinolaryngology , Shiga University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) It is pollinosis caused by Japanese cedar or cypress pollen and a final diagnosis is a done patient. (2) Patient judged that severity of symptoms when beginning to investigate is more than slight illness based on risk stratification of "Practical Guideline for the Management of Allergic Rhinitis in Japan(2009)" (3) Written informed consent is required.

Exclusion criteria

Exclusion criteria: (1) with nasal diseases such as nasal polyps, hypertrophic rhinitis, acute chronic rhinitis, or deviated septum which cause a barrier to evaluate nasal symptoms. (2) Patient that change of symptom is remarkable after specific immunotherapy is begun. (3) Patient who should continuously use medicine (antiallergic drugs, antihistamine drugs, anticholinergic drugs, a complex of histamine/ Gamma-globulin preparations, vasoconstrictor drugs and antihypertensive drugs) that influences when effect of drug evaluation. (5) Pregnancy, potential pregnancy, and breast-feeding patient. (6) the others, inappropriate to this study by the judgment of doctor.

Design outcomes

Primary

MeasureTime frame
Transitions of nasal symptom and ocular condition of two weeks after beginning of the treatment from first medical examination

Secondary

MeasureTime frame
Symptom score (stuffy nose,runny nose, sneezing,eye itchiness and tearing), medication score and QOL Questionaire score(JRQLQ No1). Satisfaction rating to treatment.

Countries

Japan

Outcome results

None listed

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