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Prospective randomized controlled study of valsartan application to promote left ventricular reverse remodeling after surgery for hypertrophic cardiomyopathy

Prospective randomized controlled study of valsartan application to promote left ventricular reverse remodeling after surgery for hypertrophic cardiomyopathy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082062
Enrollment
Unknown
Registered
2024-03-20
Start date
2023-08-02
Completion date
Unknown
Last updated
2024-03-25

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

Conditions

hypertrophic cardiomyopathy

Interventions

Group A (Betadine + Valsartan treatment group) :Betadine + Valsartan
Group B (Betadine conventional treatment group):Betadine

Sponsors

Fuwai Hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) 18 years of age or older; 2) Diagnosed with hypertrophic cardiomyopathy (basal septal hypertrophy type) requiring septal myocardial resection, with no significant surgical complications; 3) Sinus rhythm; 4) Voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1) Pregnant and lactating women; children (65 years old); 2) Valsartan or excipient allergy; 3) Previous use of ACEIs or ARBs; lithium; potassium-preserving diuretics, potassium supplements; non-steroidal anti-inflammatory drugs; 4) Diabetic patients using Aliskiren; 5) Patients with hepatic or renal insufficiency; unilateral or bilateral renal artery stenosis; cholestasis or biliary obstruction; 6) Those with severe sodium deficiency or hypovolemia; 7) History of previous cardiac surgery or chemical ablation; 8) Patients with other serious cardiac diseases or comorbidities; 9) Serious intraoperative complications; 10) Other conditions such as inability to complete one year of follow-up that the investigator considers inappropriate for participation.

Design outcomes

Primary

MeasureTime frame
Late Gadolinium Enhancement;

Secondary

MeasureTime frame
Left ventricular diastolic function;Non-sustained ventricular tachycardia;

Countries

China

Contacts

Public ContactYanhai Meng

Fuwai Hospital, Chinese Academy of Medical Sciences

mengyanhai@126.com+86 134 3921 4906

Outcome results

None listed

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