Clinical Trials Directory

Trials / Completed

CompletedNCT01529229

Comparison of Desloratadine Associated With Prednisolone Oral Solution Versus Dexchlorpheniramine Associated With Betamethasone for Persistent Allergic Rhinitis Treatment

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 Moderate - Severe Persistent Allergic Rhinitis

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
210 (actual)
Sponsor
EMS · Industry
Sex
All
Age
2 Years – 11 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the non-inferiority clinical efficacy of two different drug associations in the treatment of Moderate - Severe Persistent Allergic Rhinitis.

Detailed description

* double-blind, non-inferiority, prospective, parallel group trial. * Experiment duration: 07 days. * 02 visits (days 0 and 7). * Efficacy will be evaluated for persistent allergic rhinitis based on nasal symptoms score * Adverse events evaluation.

Conditions

Interventions

TypeNameDescription
DRUGDexchlorpheniramine + BetamethasoneChildren (2 to 5 years): 2.5 ml 3 times a day Children (6 to 12 years): 5.0 ml 3 times a day
DRUGDesloratadine + PrednisoloneChildren (2 to 5 years): 2.5 ml 3 times a day Children (6 to 12 years): 5.0 ml 3 times a day

Timeline

Start date
2013-11-01
Primary completion
2014-10-01
Completion
2014-10-01
First posted
2012-02-08
Last updated
2015-01-15

Source: ClinicalTrials.gov record NCT01529229. Inclusion in this directory is not an endorsement.