Clinical Trials Directory

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

TypeNameDescription
DRUGdesloratadinesingel dose, oral, 20 mg
DRUGdesloratadinesingle 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.

Effects of 5 mg vs. 20 mg Desloratadine on Skin Lesions in Patients With Chronic Urticaria (CU) (NCT00598611) · Clinical Trials Directory