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Not yet recruitingNCT07068633Updated Jul 16, 2025

Korea VHD Echo Study: Surveillance of Aortic, Mitral & Tricuspid Patients - Insights From Real-world Practice

An observational study in Heart Valve Diseases, Aortic Valve Stenosis and Aortic Valve Insufficiency, sponsored by Yonsei University. Not yet recruiting at 1 site in South Korea. Open to participants aged 19 Years and older. Per ClinicalTrials.gov, last updated 2025-07-16.

Sponsored by Yonsei University · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
30,000
Ages
19 Years and older
Sex
All
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Study summary

Valvular heart disease (VHD) is a growing public health concern globally, with increasing disease burden and rising interest in advanced treatment strategies such as transcatheter interventions. However, there remains a significant lack of real-world data regarding echocardiography practices, disease prevalence and progression, referral patterns, and treatment pathways. Addressing these gaps is critical for improving patient care and informing clinical decision-making.

South Korea provides a unique opportunity to conduct a nationwide retrospective echocardiographic study due to its advanced healthcare infrastructure, high patient volume, and strong tradition in clinical research. The current study aims to evaluate the real-world burden and clinical journey of patients with moderate or severe valvular disease over a 10-year period, based on echocardiographic and electronic medical record (EMR) data collected from multiple tertiary centers across the country.

Read the detailed description

This is a multicenter, retrospective observational study conducted using data from January 1, 2010 to December 31, 2020. The study will include adult patients (≥18 years old) who underwent at least two transthoracic echocardiograms during the study period. Eligible patients will be identified consecutively from each participating institution's echocardiographic and EMR databases. Patients with moderate or severe valvular heart disease (VHD), as defined by guideline-based echocardiographic criteria, will be included in the final analysis.

Patients with congenital heart disease, previous valve surgery at baseline, or incomplete clinical or imaging data will be excluded. The data collected will include demographics, comorbidities, echocardiographic parameters, and clinical outcomes such as mortality and treatment interventions. Particular attention will be paid to disease severity at baseline, rate of progression (from mild to severe), and time to treatment. Treatment patterns, including referral to surgery or transcatheter valve interventions (e.g., TAVI), will also be explored.

Sampling will follow a non-probability, consecutive patient sampling approach, as patients are retrospectively identified based on predefined eligibility criteria. The final sample size is estimated based on precedent data from a previous Korean VHD study that included \~4,000 patients over a 2-month period across 45 centers. Given the 10-year study duration and the number of participating institutions, a larger and more comprehensive sample is expected in this study.

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Conditions studied

  • Heart Valve Diseases
  • Aortic Valve Stenosis
  • Aortic Valve Insufficiency
  • Mitral Valve Insufficiency
  • Mitral Valve Prolapse
  • Tricuspid Valve Insufficiency
  • Rheumatic Heart Disease
  • Aortic Diseases
03

Who can participate

Ages eligible
19 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

This retrospective study includes adult patients (≥18 years) diagnosed with moderate or severe valvular heart disease (VHD) between January 1, 2010, and December 31, 2020, at tertiary hospitals in South Korea. Eligible patients must have undergone at least two transthoracic echocardiograms. Patients will be identified consecutively from echocardiographic and electronic medical record (EMR) databases. Exclusion criteria include congenital heart disease, prior valve surgery at baseline, and incomplete imaging or clinical data. Patients will be classified by valve type (aortic stenosis, aortic regurgitation, mitral regurgitation, tricuspid regurgitation), severity (moderate vs. severe), and etiology (degenerative, rheumatic, endocarditis, etc.). Demographic information such as age, sex, and comorbidities will be collected. The estimated sample size is expected to exceed 10,000 patients based on the number of participating centers and the 10-year study period.

Inclusion criteria

  • Period: 2010.1.1\~2020.12.31
  • Age > 18 years
  • Moderate or severe native VHD (AS, AR, MR and TR)
  • Perform echocardiography more than twice

Exclusion criteria

Exclusion Criteria:

  • Poor image of echocardiography
  • Follow up loss
04

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
30,000 participants (estimated)
Patient registry
No

Groups and cohorts

  • Aortic petients

    Primary focus is aortic stenosis patients; secondary focus is aortic regurgitation.

  • Mitral Patients

    Primary focus is Degenerative Mitral Regurgitation patients; secondary focus is Functional Mitral Regurgitation.

  • Tricuspid Patients

    Primary focus is Tircuspid Regurgitation patients

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What researchers measure

Primary outcomes

  1. Prevalence of Moderate and Severe Valvular Heart Disease (VHD)

    Evaluate the prevalence of moderate and severe VHD (including AS, AR, MR, and TR) based on echocardiographic findings and diagnostic records during the study period.

    Time frame: January 1, 2010 - December 31, 2020

  2. Etiological Classification of Aortic Stenosis (AS)

    Classify AS cases retrospectively into degenerative, bicuspid, rheumatic, infective endocarditis, or aortopathy based on clinical records and imaging data.

    Time frame: January 1, 2010 - December 31, 2020

  3. Etiological Classification of Aortic Regurgitation (AR)

    Categorize AR patients according to underlying causes: degenerative, bicuspid, rheumatic, infective endocarditis, or aortopathy.

    Time frame: January 1, 2010 - December 31, 2020

  4. Etiological Classification of Mitral Regurgitation (MR)

    Retrospectively classify MR into primary MR (degenerative, mitral valve prolapse, rheumatic, endocarditis) and secondary MR (ventricular functional MR, atrial functional MR).

    Time frame: January 1, 2010 - December 31, 2020

  5. Classification of Tricuspid Regurgitation (TR)

    Classify TR cases into primary and secondary based on echocardiographic findings and clinical context.

    Time frame: January 1, 2010 - December 31, 2020

  6. Disease Progression and Treatment Pathway

    Analyze the time course of VHD progression from mild to moderate to severe and track the time to intervention (surgical or transcatheter) using retrospective patient records.

    Time frame: January 1, 2010 - December 31, 2020

Secondary outcomes

  1. All-Cause and Cardiovascular Mortality

    Assess the incidence of all-cause mortality and cardiovascular-specific mortality among patients with valvular heart disease, using hospital records and national death registry data (if available).

    Time frame: From initial diagnosis to date of death or last follow-up (within 2010-2020)

  2. Treatment Pathway by Disease Severity

    Evaluate how the treatment approach (medical management, surgical valve repair/replacement, or transcatheter intervention) varies according to disease severity (mild, moderate, severe) across different types of VHD.

    Time frame: From initial diagnosis to date of death or last follow-up (within 2010-2020)

06

Study locations

1 site
  • Division of Cardiology, Yonsei Cardiovascular Hospital, Yonsei University College of Medicine
    Seoul, 03722, South Korea
07

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07068633
Lead sponsor
Yonsei University
Responsible party
Sponsor
First posted
Jul 16, 2025
Start date
Aug 2025 (estimated)
Primary completion
Dec 31, 2027 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Jul 16, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
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