CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 342 enrolled
Drug / intervention
Ergoferon +1 moredrug
Likely dose
Ergoferon 5 mlfrom 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/NCT01765920
NCT01765920Phase 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 Adult Patients

Materia Medica Holding·interventional·Posted Jan 10, 2013·Updated Jan 5, 2021

In Brief

A Phase 3 clinical trial evaluating Ergoferon and Placebo for Acute Upper Respiratory Tract Infections. Completed, enrolled 342 participants across 18 sites.

Detailed Summary

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

Study Details

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

Timeline

Phase 3CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedJan 10, 2013
Enrollment StartDec 1, 2012
Primary CompletionDec 1, 2014
Study CompletionApr 1, 2015
TodayJul 2, 2026
Enrollment to primary: 2 yearsPosted 13.5 years ago

Interventions

Ergoferondrug

5 ml 3 times a day

Placebodrug

5 ml 3 times a day