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The Predictive Value of Heart Rate Variability for Ventricular Arrhythmia Risk in Patients with Severe Organic Mitral Regurgitation

The Predictive Value of Heart Rate Variability for Ventricular Arrhythmia Risk in Patients with Severe Organic Mitral Regurgitation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500109027
Enrollment
Unknown
Registered
2025-09-10
Start date
2025-09-10
Completion date
Unknown
Last updated
2025-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mitral Valve Regurgitation

Interventions

Moderate to severe and severe DMR Group:None
None/trivial or mild DMR Group:None

Sponsors

Sun Yat-sen Memorial Hospital, Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Fully meeting the following criteria: (1) Age >= 18 years; (2) Outpatients or inpatients who visited Sun Yat-sen Memorial Hospital of Sun Yat-sen University between January 1, 2018, and September 30, 2024; (3) Completion of transthoracic echocardiography (TTE)/transesophageal echocardiography (TEE) during this period, with a confirmed diagnosis of moderate-to-severe or severe DMR based on comprehensive assessment of qualitative and quantitative echocardiographic indicators according to the Clinical Pathway for Transcatheter Mitral Valve Edge-to-Edge Repair in China (2022 Simplified Version) 11 (Figure 1); (4) Completion of routine electrocardiogram and ambulatory electrocardiogram during this period.

Exclusion criteria

Exclusion criteria: Meet any of the following criteria: (1) MR caused by other reasons; (2) Currently taking beta-blockers or any antiarrhythmic drugs; (3) Persistent atrial fibrillation; (4) Sick sinus syndrome; (5) Ventricular pacing proportion exceeding 10% after pacemaker implantation; (6) Combined moderate or higher aortic valve lesions; (7) Abnormal intracardiac shunt (e.g., atrial septal defect, ventricular septal defect, etc.); (8) MR caused by active infective endocarditis, acute myocardial infarction, etc., with duration less than 3 months; (9) Uncontrolled acute left heart failure; (10) Severe cardiac dysfunction (NYHA Class IV or LVEF <20%), or end-stage heart failure (ACC/AHA Stage D); (11) Untreated severe coronary artery stenosis; (12) Severe medical conditions such as severe infection, sepsis, acute exacerbation of COPD, severe hepatic or renal insufficiency, etc.; (13) Advanced cancer, rheumatic immune tissue diseases, severe infections, etc., or expected survival <1 year; (14) Pregnant or lactating patients; (15) Other reasons deemed by the investigator as unsuitable for this study.

Design outcomes

Primary

MeasureTime frame
ECG;Imaging;Various Ventricular Arrhythmias;Clinical;Biochemistry;

Countries

China

Contacts

Public ContactMaohuan Lin

Sun Yat-sen Memorial Hospital, Sun Yat-sen University

13580575861@163.com+86 135 8057 5861

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026