- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04329234
Korean Heart Failure Registry III (KorHF-III)
Korean Heart Failure Registry Ⅲ of Korean Society of Heart Failure
KorHF III is a multi-center, nationwide, prospective registry of the Korean Society of Heart Failure, which enrolls patients with acute heart failure in Korea.
The aim of this registry is to analyze the etiology, treatment, treatment, and prognosis to develop strategies for managing acute heart failure.
Study Overview
Status
Conditions
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Dong-Ju Choi, MD, PhD
- Phone Number: 82317877007
- Email: djchoi@snubh.org
Study Contact Backup
- Name: Jin Joo Park, MD, PhD
- Phone Number: 82317877074
- Email: jinjooparkmd@gmail.com
Study Locations
-
-
-
Seongnam, Korea, Republic of, 463707
- Recruiting
- Seoul National University Bundang Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
All consecutive hospitalized adult heart failure patients who fulfill one of 1-3 and 4
Inclusion Criteria:
- Symptoms of heart failure
- Signs of heart failure
- Lung congestion in Chest-x-ray
- Objective finding of structural and/or functional disorder of the heart or elevated natriuretic peptide levels
Exclusion Criteria:
- Patients younger than 18 years old
- Patients who do no consent
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
acute heart failure
Patients with acute heart failure
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
In-hospital mortality
Time Frame: 5 years
|
In-hospital mortality
|
5 years
|
Post-discharge mortality
Time Frame: 5 years
|
Post-discharge mortality
|
5 years
|
Post-discharge re-hospitalization
Time Frame: 5 years
|
Post-discharge re-hospitalization
|
5 years
|
Collaborators and Investigators
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- KorHF-III
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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