Cutaneous Hypersensitivity Clinical Trial
Official title:
A Double-blind, Randomized, Multicenter Parallel-group Study on Efficacy of Desloratadine and Prednisolone Association Compared to Dexchlorpheniramine and Betamethasone Association in Children (2-12 Years) With Acute Cutaneous Rash
The purpose of this study is to evaluate the non-inferiority clinical efficacy of two different drug associations in the treatment of acute cutaneous rash in children between 2 and 12 years old.
- double-blind, non-inferiority, prospective, parallel group trial.
- Experiment duration: 05 days.
- 03 visits (day 0, 48 hours and day 5).
- Efficacy will be evaluated for acute cutaneous rash based on symptoms score
- Adverse events evaluation.
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