A clinical trial to evaluate the effect of levocetirizine on pruritic skin diseases.
- Conditions
- Pruritic skin diseases
- Registration Number
- JPRN-UMIN000008463
- Lead Sponsor
- Department of Dermatology, Tokyo Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Not provided
1)Patients with an acute infection. 2)Patients treated with ultraviolet therapy or subcutaneous allergen-specific immunotherapy. 3)Patients treated with corticosteroid orally or injections. 4)Patients who drive a car or engaging in hazardous occupations. 5)Patients who are pregnant or possibly pregnant women, or breastfeeding women. 6)Patients who has sever complicating diseases like hepatic disease, kidney disease, hart disease. 7)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 Itch: Visual analog scale
- Secondary Outcome Measures
Name Time Method Itch: Scratch score Severity: Objective SCORAD QOL: DLQI, Skindex16 Daytime drowsiness: ESS Nocturnal sleep: Pittsburgh Sleep Quality Index (PSQI)