Ivabradine Effects in Cardiogenic Shock Requiring Inotropic Support

Last updated: October 20, 2022
Sponsor: The Young Investigator Group of Cardiovascular Research
Overall Status: Active - Recruiting

Phase

3

Condition

Heart Failure

Chest Pain

Heart Disease

Treatment

N/A

Clinical Study ID

NCT05594342
YIG-10202201
  • Ages > 18
  • All Genders

Study 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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Decompensated heart failure with reduced ejection fraction (HFrEF) admitted forcardiogenic shock requiring inotropic support.

Exclusion

Exclusion Criteria:

  • Decompensated heart failure with reduced ejection fraction (HFrEF) not requiringinotropic support.
  • Patients with no oral intake
  • Patients who refused to sign the consent

Study Design

Total Participants: 200
Study Start date:
July 01, 2022
Estimated Completion Date:
January 01, 2023

Study Description

Background and study rationale:

Ivabradine is a Heart Rate (HR) lowering agent which acts by inhibiting the If current in the sinoatrial node. It is currently indicated in patients with chronic heart failure with reduced ejection fraction (HFrEF). Dobutamine is an inotropic drug used in cardiogenic shock patients and it is associated with an increase in HR and incidence of cardiac arrhythmias.2 However, studies have suggested that increased heart rate may be deleterious in decompensated HFrEF due to an inverted Bowditch-Treppe response. Data regarding the safety and efficacy of ivabradine use in severely decompensated HFrEF requiring inotropic support is limited to case series.1, 2

Aim of the work:

  • This study aims to evaluate ivabradine safety and tolerability in admitted cardiogenic shock patients who started on dobutamine infusion for inotropic support.

  • Design: Randomized open-label interventional clinical trial.

Methods and patients:

  • Study Type: Interventional (Clinical Trial)

  • Estimated Enrollment: 200 participants

  • Allocation: Randomized

  • Perspective: Prospective Study

  • Intervention Model: Two Group Assignment

  • Masking: None (Open Label)

  • Primary purpose: Treatment

  • Official title: Ivabradine effects in cardiogenic shock requiring inotropic support (IVA-CS)

  • Start Date: 01 August 2022

  • Estimated Primary Completion Date: 01 January 2023

Connect with a study center

  • Andalusia Hospitals

    Alexandria, 21521
    Egypt

    Site Not Available

  • Tiba Hospital

    Alexandria, 21521
    Egypt

    Active - Recruiting

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