A study evaluating efficacy of non-sedative antihistamine up-titration in patients with chronic urticaria who did not respond to standard therapy.
Not Applicable
- Conditions
- chronic urticaria
- Registration Number
- JPRN-UMIN000008062
- Lead Sponsor
- on-Profit Organization Health Institute Research of Skin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 200
Inclusion Criteria
Not provided
Exclusion Criteria
1) Patients with a known allergy to any component of the study drug. 2) Pregnant or possibly pregnant women, or breastfeeding women. Women who wish to become pregnant during study participation. 3) Patients who are judged inappropriate to participate in the study by the investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method - Improvement in the degree of itching in the daytime and nighttime
- Secondary Outcome Measures
Name Time Method - Improvement in the duration of rash - Improvement in the degree of skin eruption (erythema, wheal, area/ extent) - Change in QOL (Skindex-16) - Overall improvement rating (degree of skin eruption, degree of itching) - Degree of satisfaction regarding efficacy - Safety