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Study Comparing 3 Formulations to Evaluate the Efficacy and Safety of the Inflammatory Symptoms of Superior Air Passages Affection, in Children Between 2 and 6 Years Old

2014-08-27 03:19:43 | BioPortfolio

Summary

The primary outcome of this study is to evaluate the clinical efficacy of the dose fixed combination and each drug, that composes it, isolated, regarding the respiratory symptoms improvement in superior air passages acute affection in children between 2 and 6 years old.

Study Design

Allocation: Randomized, Control: Active Control, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Conditions

Common Cold

Intervention

Bronpheniramine and fenilefrine (Decongex Plus), Bronpheniramine isolated, Fenilefrine isolated

Location

Unifesp
São Paulo
SP
Brazil

Status

Not yet recruiting

Source

Ache Laboratorios Farmaceuticos S.A.

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:19:43-0400

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