drugset / Trial / NCT05594342

Ivabradine Effects in Cardiogenic Shock Requiring Inotropic Support

NCT05594342

RandomizedParallel-groupOpen-labelTreatment

Summary

Data regarding the safety and efficacy of ivabradine use in severely decompensated HFrEF requiring inotropic support is limited to case series.1 This study aimed to evaluate ivabradine safety and tolerability in admitted cardiogenic shock patients who started on dobutamine infusion for inotropic support.

Timeline

Start
2022-07-01
Primary completion
2023-01-01
Completion
2023-01-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Ivabradine Small molecule 7.5 mg Oral
Background Dobutamine Small molecule