- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07601022
Acute Heart Failure Registry (B-AHF)
May 28, 2026 updated by: Jin Joo Park
Clinical Utility of Quantitative Electrocardiography in Patients With Acute Heart Failure: A Prospective Observational Study
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.
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
400
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Gyeonggi-do
-
Seongnam-si, Gyeonggi-do, South Korea, 13620
- Recruiting
- Seoul National University Bundang Hospital
-
Contact:
- Jin Joo Park, MD, PhD
- Phone Number: +82-317877074
- Email: jinjooparkmd@gmail.com
-
Contact:
- Minjae Yoon, MD
- Phone Number: +82317877854
- Email: minjae1677@gmail.com
-
Sub-Investigator:
- Minjae Yoon, MD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients with acute heart failure who were admitted to the hospital
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
1-year mortality
Time Frame: From enrollment to 1-year
|
From enrollment to 1-year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
LVEF change
Time Frame: From enrollment to 1-year
|
LVEF change by echocardiography
|
From enrollment to 1-year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 8, 2026
Primary Completion (Estimated)
December 31, 2030
Study Completion (Estimated)
December 31, 2030
Study Registration Dates
First Submitted
May 15, 2026
First Submitted That Met QC Criteria
May 15, 2026
First Posted (Actual)
May 22, 2026
Study Record Updates
Last Update Posted (Actual)
June 1, 2026
Last Update Submitted That Met QC Criteria
May 28, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- B-2512-1016-301
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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