drugset / Trial / NCT02166060

Ivabradine in Patients With an Unsatisfactory Percentage of Cardiac Resynchronization Therapy

NCT02166060

Phase 4 Unknown 60 enrolled Medical University of Warsaw
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the role of ivabradine in cardiac resynchronization recipients with an unsatisfactory percentage biventricular pacing. The study protocol 60 patients with heart failure NYHA (New York Heart Association) II-IV treated with optimal medical therapy as clinically indicated who received CRT-D device more than 3 months ago. Patients with biventricular pacing \<95% will and heart rate \<70 at rest and \>50% of heart rate in device memory \>70 will receive ivabradine. The minimal follow-up of patients in the study will be at least six months.

Timeline

Start
2014-08
Primary completion
2016-08
Completion
2016-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Ivabradine Small molecule 5 mg
Subject Ivabradine Small molecule 7.5 mg

Indications