Study of medication timing of levocetirizine dihydrochloride in patients with recalcitrant chronic urticaria to anti-histamine drug
Not Applicable
- Conditions
- Chronic urticaria
- Registration Number
- JPRN-UMIN000013777
- Lead Sponsor
- Department of Dermatology, Kurume University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
1. Patients with acute infectious disease 2. Patients who are treated with ultra-violet therapy or hyposensitization therapy 3. Patients who engaged in dangerous job such as driving a car 4. Patients who were treated with systemic steroids less than 2 weeks prior to the initiation of this study 5. Patients who are pregnant or has possibility to be pregnant, and who are lactating 6. Patients who suffered from grave liver, renal, or heart disease 7. Patients who do not have hypertension, diabetes mellitus, or collagen disease 8. Patients who are considered inappropriate to be enrolled in this study by the doctor
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method degree of pruritus
- Secondary Outcome Measures
Name Time Method adverse event