drugset / Trial / NCT00967759
Study Comparing 3 Formulations to Evaluate the Efficacy and Safety of the Inflammatory Symptoms of the Upper Respiratory Tract, in Children Between 2 and 6 Years Old
RandomizedParallel-groupTriple-blindTreatment
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.
Timeline
- Start
- —
- Primary completion
- —
- Completion
- —
Outcome
Outcome not reported
Stopped: “The study was designed again in compliance with the regulatory agency.”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Bronpheniramine | Unknown | 2 mg/ml | Oral |
| Comparator | Fenilefrine | Unknown | 2.5 mg/ml | Oral |