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An early intervention study of left ventricular diastolic function in obese hypertensive patients based on volume index

An early intervention study of left ventricular diastolic function in obese hypertensive patients based on volume index

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071759
Enrollment
Unknown
Registered
2023-05-24
Start date
2023-06-01
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

hypertension

Interventions

treatment group:Azisartan 40mg qd oral
control group:Amlodipine besylate 5mg qd

Sponsors

China-Japan Friendship Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. The age is 18-70 years old (including 18 and 70 years old), and the gender is not limited; 2. BMI >= 28kg/m2 (BMI= weight/height 2); 3. Patients diagnosed with grade 1 and grade 2 essential hypertension (SBP >= 140mmHg and/or DBP >= 90mmHg and SBP 14; LAVI > 34 mL/m2; TR > 2.8m/s meets both criteria).

Exclusion criteria

Exclusion criteria: 1. Secondary hypertension (renal parenchymatous hypertension, Cushing's syndrome, primary aldosteronism, pheochromocytoma, drug-induced hypertension, etc.); 2. Mean sitting blood pressure >= 180 mmHg and/or DBP >= 110mmHg, or patients with acute hypertension or subacute hypertension; 3. Allergy to CCBS or ARBS, and intolerance to amlodipine or azisartan ester (e.g. Angioedema); 4. Secondary obesity: hypercortisolism, hypothyroidism; 5. Severe arrhythmia and atrial fibrillation; 6. Coronary heart disease, heart failure, valvular heart disease, pulmonary heart disease, congenital heart disease, cardiomyopathy, hyperthyroid heart disease; 7. Diabetes mellitus; 8. Cerebrovascular diseases; 9. Patients with obvious clinical manifestations or signs of liver disease or screening visits with ALT > 2.5 x UNL and/or AST > 2.5 x UNL and/or total bilirubin > 1.5 x UNL; Severe renal dysfunction, eGFR = 35); 12. Patients deemed unsuitable for clinical study.

Design outcomes

Primary

MeasureTime frame
Left atrial volume index;

Secondary

MeasureTime frame
Global long axial strain of left ventricle;NT-proBNP;

Countries

China

Contacts

Public ContactChen Gailing

China-Japan Friendship Hospital

chengailing33@163.com+86 136 2138 6083

Outcome results

None listed

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