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Starting soon Observational

Are Carvedilol and Metoprolol Succinate Comparable Treatments in Heart Failure Patients With Reduced Ejection Fraction

NCT04996550 · tracked via the Priya Life Science Denmark tracker
Phase
Observational
Started
2022-01-03
Last updated
2021-08-16

Condition(s) studied

Chronic Heart Failure

Investigational drug(s) / intervention(s)

Carvedilol →Metoprolol Succinate →

Carvedilol: To compare the efficacy of carvedilol and metoprolol succinate on all-cause mortality or first hospitalization for worsening heart failure in patients with heart failure with reduced ejection fraction with an indication for treatment with beta-blockers.

Metoprolol Succinate: To compare the efficacy of carvedilol and metoprolol succinate on all-cause mortality or first hospitalization for worsening heart failure in patients with heart failure with reduced ejection fraction with an indication for treatment with beta-blockers.

Study summary

The objective of CROWD-COMPARE is to compare the efficacy of carvedilol and metoprolol succinate on all-cause mortality or first hospitalization for worsening heart failure in patients with heart failure with reduced ejection fraction with an indication for treatment with beta-blockers.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥18 years * NYHA ≥ II * LVEF ≤40% Exclusion Criteria: * No indication for beta-blocker treatment or contraindications for the two for the two study drugs (Carvedilol or metoprolol succinate)

Primary outcome measure(s)

  • A combined endpoint of all-cause mortality or first hospitalization for worsening heart failure. — Four years with randomized cluster allocation and two year of follow-up.
    To compare the efficacy of carvedilol and metoprolol succinate in patients with heart failure with reduced ejection fraction with an indication for treatment with beta-blockers.

Trial sites (1)

FacilityCityRegionStatus
Department of Cardiology, Odense University Hospital Odense Region Syddanmark
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04996550 on ClinicalTrials.gov ↗ ← All trials in Denmark