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Effect of ARNI on cardiac diastolic function and short-term heart rate variability in patients with hypertensive heart disease

Effect of ARNI on cardiac diastolic function and short-term heart rate variability in patients with hypertensive heart disease or hypertrophic cardiomyopathy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400088330
Enrollment
Unknown
Registered
2024-08-15
Start date
2023-02-11
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

hypertension

Interventions

hypertension study group: ARNI :None
hypertension control group: valsartan:None

Sponsors

The First Affiliated Hospital of the Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
31 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for the HHD group: 1. age 18-75 years old and gender; 2. previous history of hypertension with clinical diagnosis of HHD: no antihypertensive medication, office blood pressure (systolic blood pressure =140 mmHg and/or diastolic blood pressure =90 mmHg); combined with the following (1) signs or symptoms of heart failure; and/or (2) confirmed cardiac enlargement, diagnostic criteria of echocardiography: left ventricular hypertrophy and enlargement, enlarged left atrium, aortic hypoelasticity, and A-peak > E-peak (A Echocardiographic diagnostic criteria: left ventricular hypertrophy, enlargement, left atrial enlargement, aortic hypoelasticity, peak A > peak E (A > E), can diagnose HHD; 3. echocardiographic measurement of cardiac data left ventricular ejection fraction (LVEF) =50%; 4. systolic blood pressure 35 mm; b. left atrial volume index >21 ml/m2 (men) and left atrial volume index >22 ml/m2 (women); and/or septal thickness or left ventricular posterior wall thickness =1.1 cm and =2.5 cm), corrected for the actual situation in China; 6. patients volunteered to participate in the study and their informed consent was obtained; 7. the control group was selected to match the study group in terms of gender and age, etc. HHD without other heart diseases and other causes of ventricular hypertrophy and diastolic dysfunction after inquiring about the medical history and relevant examinations;

Exclusion criteria

Exclusion criteria: Exclusion criteria for HHD group: 1. physiologic left atrial volume increase in athletes; 2. patients with history of angioedema, estimated glomerular filtration rate (eGFR) 145 mmol/L) or potassium concentrations (5.5 mmol/L); 5. life-threatening or uncontrolled arrhythmias, including symptomatic or sustained ventricular tachycardia and atrial fibrillation or atrial flutter with a resting ventricular rate >110 beats per minute;

Design outcomes

Primary

MeasureTime frame
Left ventricular diastolic function;Short range heart rate variability;

Secondary

MeasureTime frame
Baseline indicators: blood pressure, weight, uric acid, etc;

Countries

China

Contacts

Public ContactHouyuan Hu

The First Affiliated Hospital of the Army Medical University

huhouyuan@qq.com+86 173 8308 1654

Outcome results

None listed

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