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Recruiting NCT07601022

Acute Heart Failure Registry

— Observational Acute Heart Failure (AHF)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Acute Heart Failure (AHF). Basic parameters: from 19 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
South Korea
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Clinical Utility of Quantitative Electrocardiography in Patients With Acute Heart Failure: A Prospective Observational Study

Overview

To evaluate the clinical utility of quantitative electrocardiography (Quantitative ECG, QCG) by analyzing its associations with clinical characteristics and laboratory findings in patients hospitalized with acute heart failure.

Primary outcome measures

  • 1-year mortality [Time frame: From enrollment to 1-year]
Secondary outcome measures (1)
  • LVEF change [Time frame: From enrollment to 1-year]

Eligibility criteria

Inclusion criteria

  • Adults aged 19 years or older who were admitted to the Department of Cardiology for acute heart failure
  • NT-proBNP ≥300 pg/mL
  • Patients who underwent electrocardiography at least once

Exclusion criteria

  • History of congenital heart disease
  • Patients with a dominant electronic pacemaker rhythm
  • Patients with a heart rate >140 beats per minute or electrocardiograms with excessive noise

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

South Korea · 1 center
  • Seoul National University Bundang Hospital — Seongnam-si

Identifiers

NCT: NCT07601022 · B-2512-1016-301

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗