CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 306 enrolled
Drug / intervention
Ergoferon +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01843842
NCT01843842Phase 3Completed

Multicentre Double-blind Placebo-controlled Parallel-group Randomized Clinical Trial of Safety and Clinical Efficacy of Ergoferon in Liquid Dosage Form in Treatment of Acute Upper Respiratory Tract Infections in Children

Materia Medica Holding·interventional·Posted May 1, 2013·Updated Nov 29, 2018

In Brief

A Phase 3 clinical trial evaluating Ergoferon and Placebo for Acute Upper Respiratory Tract Infections. Completed, enrolled 306 participants across 11 sites.

Detailed Summary

The purpose of this study is: * to assess safety of the liquid dosage form of Ergoferon for treatment of acute upper respiratory tract infections in children; * to assess clinical efficacy of the liquid dosage form of Ergoferon for treatment acute upper respiratory tract infections in children.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesRussia
Collaborators--

Timeline

Phase 3CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedMay 1, 2013
Enrollment StartApr 1, 2013
Primary CompletionMar 1, 2015
TodayJul 2, 2026
Enrollment to primary: 1.9 yearsPosted 13.2 years ago

Interventions

Ergoferondrug

Safety and Efficiency of liquid dosage form

Placebodrug

Safety and Efficiency of liquid dosage form