CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 6,505 enrolled
Drug / intervention
Ivabradine +1 moredrug
Likely dose
Ivabradine 2.5mgfrom 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/NCT02441218
NCT02441218Phase 3Completed

Effects of Ivabradine on Cardiovascular Events in Patients With Moderate to Severe Chronic Heart Failure and Left Ventricular Systolic Dysfunction. A Three-year International Multicentre Study

Institut de Recherches Internationales Servier·interventional·Posted May 12, 2015·Updated Jan 3, 2020

In Brief

A Phase 3 clinical trial evaluating Ivabradine and Placebo for Chronic Heart Failure. Completed, enrolled 6,505 participants across 2 sites in 2 countries.

Detailed Summary

The primary objective of this study is to demonstrate the superiority of ivabradine over placebo in the reduction of cardiovascular mortality or hospitalisation for worsening heart failure in patients with moderate to severe symptoms of chronic heart failure, a reduced left ventricular ejection fraction and currently receiving recommended therapy for this disease.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesFrance, Sweden
Collaborators--

Timeline

Phase 3CompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMay 12, 2015
Enrollment StartSep 1, 2006
Primary CompletionApr 1, 2010
TodayJul 2, 2026
Enrollment to primary: 3.6 yearsPosted 11.1 years ago

Interventions

Ivabradinedrug

2.5mg, 5mg or 7.5mg tablets to be taken orally twice daily, at 12-hours intervals, in the morning and in the evening during meals up to 42 months.

Placebodrug

Matching placebo tablets to be taken orally twice daily, at 12-hours intervals, in the morning and in the evening during meals up to 42 months.