Randomized, double blind, crossover clinical study to evaluate the sedative effect after the treatment of 1 mg dose of ketotifen, or 10 or 20 mg dose of cetirizine using saccadic eye movement analysis in healthy male volunteers
Not Applicable
- Conditions
- allergic rhinitis, pollen allergy
- Registration Number
- JPRN-UMIN000004527
- Lead Sponsor
- Department of Clinical Pharmacy, School of Pharmacy, Showa University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Male
- Target Recruitment
- 6
Inclusion Criteria
Not provided
Exclusion Criteria
1.Subjects who have inappropriate medical history (ex., drug abuse, alcoholism, any kind of heart, liver, kidney, lung, eye and blood diseases etc.) or who are ingested medicine during this study. 2.Smoker. 3.Any drug allergy. 4.Subjects who are using excessive alcohol regularly (cannot keep abstinence for study period) 5.Nocturnal habits during night. 6.Participation in any clinical trial within the last 3 months. 7.Subjects who are inadequate for enrollment judged by the investigators.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method