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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06282822
Other study ID # HFpEF-SWE
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date March 1, 2024
Est. completion date March 1, 2025

Study information

Verified date February 2024
Source First Hospital of China Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The diagnosis of heart failure with preserved ejection fraction (HFpEF) is often complex. Echocardiography has the advantages of being a non-invasive, simple operation, low price, and high repeatability, and is of great value in the diagnosis of HFpEF. However, the current echocardiographic assessment of left ventricular diastolic dysfunction and elevated filling pressure is based on multi-parameter indirect judgment, and new parameters are urgently needed to achieve accurate judgment of left ventricular diastolic function and an accurate diagnosis of HFpEF. Myocardial stiffness refers to the ability of the myocardium to undergo stress and strain. It is an important part of the pathophysiology of cardiac diastolic dysfunction and an important parameter for clinical evaluation of the diastolic function of HFpEF. Shear-wave elastography is a novel ultrasound-based elastography technology. Based on the shear wave generated by the remote induction of the radiation force of the focused ultrasound beam, the hardness of myocardial tissue can be measured quantitatively, locally, and noninvasively, and the change in myocardial stiffness in patients with HFpEF can be directly reflected. Currently, no relevant studies have applied shear-wave elastography to the diagnosis of HFpEF. This study aims to identify changes in myocardial stiffness measured by shear-wave elastography in patients with HFpEF based on a multicenter study and apply myocardial stiffness parameters to the diagnosis of HFpEF.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 800
Est. completion date March 1, 2025
Est. primary completion date October 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Age =18 years old 2. Clear epidemiological and population characteristics of HFpEF 3. Symptoms and/or signs of heart failure 4. Echocardiographic examination of LVEF=50% 5. Objective evidence of cardiac structural and/or functional abnormalities consistent with left ventricular diastolic dysfunction and/or elevated left ventricular filling pressure, including elevated levels of natriuretic peptides 6. HFpEF score =6 or HFA-PEFF score =5 Exclusion Criteria: Any one item per patient was excluded from the study: 1. Arrhythmia. 2. ischemic heart disease. 3. Valvular heart disease or congenital heart disease with severe hemodynamic changes. 4. History of pacemaker implantation or other cardiac surgery. 5. Poor ultrasonic image quality cannot meet the parameter measurement and analysis.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Transthoracic echocardiography
All enrolled patients underwent noninvasive transthoracic echocardiography.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
First Hospital of China Medical University

Outcome

Type Measure Description Time frame Safety issue
Primary Shear wave velocity Completed within 2 weeks of enrollment
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