- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05068934
The Relationship Between Epicardial Fat Tissue and Cardiac Function in HFpEF Patients
December 31, 2025 updated by: Dongying Zhang
The Relationship Between Epicardial Fat Tissue and Cardiac Function in HFpEF
Heart failure with preserved ejection fraction (HFpEF) refers to a group of symptoms and signs of heart failure, normal or near-normal left ventricular systolic function (EF>50%), and ventricular muscle diastolic dysfunction and A clinical syndrome characterized by decreased compliance and increased stiffness.
The pathogenesis of HFpEF is related to impaired lipid metabolism and inflammation.
Epicardial adipose tissue (Epicardial Adipose tissue, EAT) is a kind of visceral adipose tissue.
Related studies have shown that extracardiac Membrane fat is related to inflammation markers, cardiometabolic risk and cardiovascular disease.However, there is still no research investigating the the relationship between epicardial fat thickness and Cardiac Function in HFpEF patients.
Study Overview
Status
Completed
Detailed Description
Heart failure with preserved ejection fraction (HFpEF) refers to a group of symptoms and signs of heart failure, normal or near-normal left ventricular systolic function (EF>50%), and ventricular muscle diastolic dysfunction and A clinical syndrome characterized by decreased compliance and increased stiffness.
The pathogenesis of HFpEF is related to impaired lipid metabolism and inflammation.
Epicardial adipose tissue (Epicardial Adipose tissue, EAT) is a kind of visceral adipose tissue, which is composed of adipose tissue deposited between the myocardium and the visceral layer of the pericardium.
It is closely adjacent to the coronary arteries and myocardium.
Related studies have shown that extracardiac Membrane fat is related to inflammation markers, cardiometabolic risk and cardiovascular disease.However, there is still no research investigating the the relationship between epicardial fat thickness and Cardiac Function in HFpEF patients.
This study intends to observe the relationship between epicardial fat thickness and left and right functions in patients with HFpEF, and evaluate whether epicardial fat thickness can be used as an indicator of left and right dysfunction.
Study Type
Observational
Enrollment (Actual)
1083
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
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Chongqing, China
- The First Affiliated Hospital of Chongqing Medical University
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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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Heart failure patients with preserved ejection fraction (HFpEF)
Description
Inclusion Criteria:
- Adult aged >=18years old;
- Diagnosed with HFpEF.
Diagnostic criteria including:
- left ventricular ejection fraction ≥50%;
- with the symptoms and/or signs of heart failure;
- BNP≥35 pg/mL and/or NTproBNP≥125 pg/mL;
- at least one additional criterion: relevant structural heart disease(LVH and/or LAE) or diastolic dysfunction
Exclusion Criteria:
- LVEF less than 45% at any time;
- Severe liver failure;
- Primary pulmonary hypertension;
- Age <18 years old.
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 |
Measure Description |
Time Frame |
|---|---|---|
|
Epicardial Fat Tissue
Time Frame: On admission
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Epicardial Fat Tissue by cardiac color Doppler ultrasound
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On admission
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|
Cardiac Function
Time Frame: On admission
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Left ventricular diastolic function and right ventricular systolic function by cardiac color Doppler ultrasound
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On admission
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Composite Endpoint of Worsening Heart Failure Event and Cardiovascular Death
Time Frame: From date of discharge until the date of first worsening HF event or date of death, whichever came first, assessed up to 5 years
|
Composite Endpoint of Worsening Heart Failure Event and Cardiovascular Death
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From date of discharge until the date of first worsening HF event or date of death, whichever came first, assessed up to 5 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Worsening HF Event
Time Frame: From date of discharge until the date of first worsening HF event or date of death, whichever came first, assessed up to 5 years
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Worsening Heart Failure Event
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From date of discharge until the date of first worsening HF event or date of death, whichever came first, assessed up to 5 years
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|
CV Death
Time Frame: From date of discharge until the date of death, whichever came first, assessed up to 10 years
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Cardiovascular Death
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From date of discharge until the date of death, whichever came first, assessed up to 10 years
|
|
All-cause Death
Time Frame: From date of discharge until the date of death, whichever came first, assessed up to 10 years
|
Death from any causes
|
From date of discharge until the date of death, whichever came first, assessed up to 10 years
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Dongying Zhang, doctor, First Affiliated Hospital of Chongqing Medical University
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)
October 12, 2020
Primary Completion (Actual)
December 10, 2025
Study Completion (Actual)
December 15, 2025
Study Registration Dates
First Submitted
September 26, 2021
First Submitted That Met QC Criteria
September 26, 2021
First Posted (Actual)
October 6, 2021
Study Record Updates
Last Update Posted (Estimated)
January 6, 2026
Last Update Submitted That Met QC Criteria
December 31, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020-09
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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