Trials / Completed
CompletedNCT00598611
Effects of 5 mg vs. 20 mg Desloratadine on Skin Lesions in Patients With Chronic Urticaria (CU)
An Exploratory Phase III, Randomised, Double-blind, Therapeutic Single Dose-related Effect, Parallel Group Study to Assess and Compare the Effects of 5 mg vs. 20 mg Desloratadine on Skin Lesions in Patients With Chronic Urticaria (CU)
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 29 (actual)
- Sponsor
- Charite University, Berlin, Germany · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare urticaria lesions (size, kinetics) by thermography, volumetry and digital time lapse photography in CU patients treated with desloratadine 5 mg or desloratadine 20 mg. Hypothesis: Updosing of desloratadine (20mg) is more efficient in the treatment of urticarial lesions as compared to standard dosing (5 mg desloratadine).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | desloratadine | singel dose, oral, 20 mg |
| DRUG | desloratadine | single dose, oral, 5 mg |
Timeline
- Start date
- 2007-09-01
- Primary completion
- 2009-08-01
- Completion
- 2009-08-01
- First posted
- 2008-01-22
- Last updated
- 2012-05-31
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT00598611. Inclusion in this directory is not an endorsement.