CROWD-COMPAREComparison of Carvedilol and Metoprolol Succinate in Heart Failure Patients With Reduced Ejection Fraction
This study aims to compare the effectiveness of carvedilol and metoprolol succinate in heart failure patients with reduced ejection fraction, by observing the combined outcome of all-cause mortality or first hospitalization for worsening heart failure.
Data Collection
Collected from today forward - ProspectiveCohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Summary
Study start date: January 3, 2022
Actual date on which the first participant was enrolled.Heart failure with reduced ejection fraction (HFrEF) is a condition that affects 1-2% of adults, increasing to over 10% in people over 70. It significantly reduces life expectancy, physical capacity, and quality of life. The CROWD-COMPARE study aims to compare the effectiveness of two beta-blockers, carvedilol and metoprolol succinate, in treating HFrEF. Beta-blockers are recommended for HFrEF patients as they can reduce symptoms, improve heart function, increase physical capacity, and decrease hospitalizations and mortality. However, there's debate over whether all beta-blockers are equally effective or if one is superior. This study is important as it could help clarify this issue and improve treatment for HFrEF patients. In the CROWD-COMPARE study, each participating cardiology department will have four periods: two with carvedilol as the primary beta-blocker and two with metoprolol succinate. The departments will be randomly assigned to start with either carvedilol or metoprolol succinate, then alternate annually. Treatment will follow Danish and European guidelines, with beta-blockers given to patients with symptomatic heart failure and a left ventricular ejection fraction (LVEF) of less than or equal to 40%. The beta-blockers will be increased to the target dose or the maximum tolerated dose. No extra patient visits will be required due to the study. Data will be collected from national registries and linked in anonymous form to hospital admissions, diagnoses, vital status, and other relevant information.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.5600 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Department of Cardiology, Odense University Hospital
Odense, DenmarkOpen Department of Cardiology, Odense University Hospital in Google Maps