Actively Recruiting

Age: 18Years +
All Genders
NCT07439159

Echocardiography-Based Predictors of Outcomes in Hospitalized Patients With Decompensated Heart Failure (ECHO-DECOMP)

Led by Istanbul University - Cerrahpasa · Updated on 2026-02-27

76

Participants Needed

1

Research Sites

178 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Acute decompensated heart failure is a leading cause of hospitalization and is associated with high morbidity and mortality. Early risk stratification in this population is crucial for guiding treatment strategies and predicting short- and long-term clinical outcomes. Transthoracic echocardiography is routinely performed in patients hospitalized with acute decompensated heart failure and provides comprehensive information regarding cardiac structure and function. However, the prognostic value of detailed echocardiographic parameters obtained before the initiation of intravenous diuretic therapy has not been fully clarified. The objective of this prospective study is to evaluate the prognostic significance of transthoracic echocardiographic findings obtained at hospital admission, prior to intravenous diuretic therapy, in patients hospitalized with acute decompensated heart failure. The study will assess key echocardiographic parameters reflecting left and right heart structure and function, including left ventricular ejection fraction, left ventricular dimensions and geometry, left atrial size and volume, indices of right ventricular systolic function (such as TAPSE, tissue Doppler-derived S' velocity, and fractional area change), pulmonary artery systolic pressure, right ventricular-pulmonary artery coupling assessed by the TAPSE/PASP ratio, and right ventricular outflow tract acceleration time. Primary outcome measures include in-hospital mortality, post-discharge mortality, myocardial infarction, ischemic stroke, and heart failure-related rehospitalization. Secondary outcomes include the need for non-invasive or invasive mechanical ventilation during hospitalization, requirement for inotropic support, changes in B-type natriuretic peptide levels, development of acute kidney injury, and occurrence of new-onset cardiac arrhythmias. By prospectively evaluating echocardiographic parameters and their associations with clinical outcomes, this study aims to clarify the prognostic role of early echocardiographic assessment in acute decompensated heart failure and to contribute to improved risk stratification and clinical decision-making in this high-risk population.

CONDITIONS

Official Title

Echocardiography-Based Predictors of Outcomes in Hospitalized Patients With Decompensated Heart Failure (ECHO-DECOMP)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 2518 years.
  • Hospitalized due to acute decompensated heart failure.
  • Intravenous diuretic therapy required as determined by a cardiologist.
  • Predominant left-sided heart failure.
  • Provided written informed consent before participation.
Not Eligible

You will not qualify if you...

  • Severe anemia with hemoglobin less than 7 g/dL.
  • Need for renal replacement therapy such as hemodialysis or peritoneal dialysis, or listed for kidney transplantation.
  • Severe primary mitral regurgitation.
  • Severe aortic stenosis.
  • Severe aortic regurgitation.
  • Severe primary tricuspid regurgitation.
  • Primary right heart failure.
  • Heart failure caused by congenital heart disease.
  • History of mitral valve replacement.
  • History of aortic valve replacement.
  • History of bioprosthetic valve replacement.
  • History of transcatheter aortic valve implantation.
  • Active malignancy.
  • Did not provide written informed consent.
  • Unable to undergo transthoracic echocardiography before intravenous diuretic therapy for any reason.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Istanbul University Cerrahpaşa Institute of Cardiology

Istanbul, Turkey (Türkiye)

Actively Recruiting

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Research Team

A

Aybike G Taşdelen Acar, MD

CONTACT

Ü

Ümit Acar, MD

CONTACT

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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