A clnical study to assess inhibitory effect of bepotastine besilate OD tablet to compare with fexofenadine hydrochloride and pseudoephedrine hydrochloride combination tablet in patients with cedar pollinosis in the OHIO Chamber.
Not Applicable
- Conditions
- Japanese cedar Pollinosis
- Registration Number
- JPRN-UMIN000010687
- Lead Sponsor
- Samoncho Clinic
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 56
Inclusion Criteria
Not provided
Exclusion Criteria
1)Patients with mucosal lesion of the nose and eyes. 2)Patients with severe or requiring treatment needed Allergic Rhinitis. 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 anaphylaxis with these drugs. 7)Patients with pregnancy, delivery or lactation.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Subjective symptoms
- Secondary Outcome Measures
Name Time Method asal secretion volume Number of sneezing Exercise-based treatment programs