Actively Recruiting
Lesser Poland Cracovian Heart Failure Registry
Led by Jagiellonian University · Updated on 2024-03-06
2500
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are conducting the Lesser Poland Cracovian Heart Failure Registry (LECRA-HF) to improve understanding of acute heart failure (AHF) and its long-term outcomes. The study aims to assess the prognosis of AHF and its influencing factors, identify optimal treatment approaches, evaluate the role of invasive coronary diagnostics and revascularization, and analyze specific heart failure subtypes, including HFimpEF, HFpEF, HFsnEF, HFrEF, and HFmrEF. This registry addresses the need for more reliable data on this diverse patient population, particularly within the Polish context. The LECRA-HF registry includes patients hospitalized with acute heart failure who are over 18 years old. Participants are categorized into three groups based on left ventricular ejection fraction (LVEF) according to European Society of Cardiology guidelines: reduced (LVEF ≤40%), mildly reduced (LVEF 41-49%), and preserved (LVEF ≥50%) ejection fraction. The registry is continuous and will be updated annually until 2026 to capture comprehensive data. During the study, detailed clinical information will be collected, including medical history, physical measurements, electrocardiograms, imaging, laboratory tests, and treatments during hospitalization and after discharge. Researchers will analyze the long-term prognosis, including all-cause mortality, cardiovascular mortality, and heart failure rehospitalizations over two years. This thorough data collection supports better characterization of heart failure subtypes and informs future treatment strategies.
CONDITIONS
Brief Title
Lesser Poland Cracovian Heart Failure Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Hospitalization due to acute heart failure
- Age over 18 years
You will not qualify if you...
- Unable to give informed consent to participate in the registry
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 2 years
Participants who undergo routine care are observed with clinical, electrocardiographic, imaging, and laboratory tests during hospitalization and after discharge.
Annual visits for up to 2 years
Trial Site Locations
Total: 1 location
1
Department of Coronary Disease and Heart Failure, John Paul II Hospital in Krakow, Jagiellonian University Medical College
Krakow, Poland, 31-202
Actively Recruiting
Research Team
K
Konrad Stępień, MD
K
Karol Nowak, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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