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To evaluate the application of Sacubitril Valsartan Sodium Tablets (LCZ696) in the early stage of acute myocardial infarction

To evaluate the application of Sacubitril Valsartan Sodium Tablets Shakubatur /Mushartan (LCZ696) in the early stage of acute myocardial infarction

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100042337
Enrollment
Unknown
Registered
2021-01-19
Start date
2021-02-15
Completion date
Unknown
Last updated
2021-04-19

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

Conditions

acute myocardial infarction

Interventions

1:Sacubitril/Valsartan
2:Valsartan

Sponsors

The Seventh People's Hospital of Zhengzhou
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years; 2. Patients diagnosed as spontaneous AMI according to the guidelines, onset within 7 days; 3. Hemodynamic stability: SBP >= 100 mmHg in patients treated with ACEI/ARB within 24 hours before randomized; Randomized patients who were not treated with ACEI/ARB drugs in the first 24 hours had SBP >= 110 mmHg; Diuretics, vasodilators, vasopressors, and/or positive inotropic agents were not used within 24 hours prior to randomization.

Exclusion criteria

Exclusion criteria: 1. Patients with a prior history of chronic heart failure were randomized; 2. Patients were randomized to the first 24 hours of cardiogenic shock; 3. Randomized patients with persistent heart failure; 4. Myocardial infarction patients planning CABG; 5. The clinical presentation is obvious in patients with right ventricular MI; 6. Symptomatic hypotension was present at screening; 7. A history of angioedema in a patient; 8. Patients with known or suspected bilateral renal artery stenosis; 9. Patients with apparent obstructive cardiomyopathy; 10. Patients who have recently undergone or are planning to undergo cardiac surgery; 11. eGFR = 5.2mmol/L at random(or hyperkalemia); 13. A history of liver damage or fibrosis is known; 14. LCZ696 history of use; 15. Cancer patients; 16. Allergy, intolerance or contraindications to ACEI/ARB/NEPI; 17. Pregnancy or lactation.

Countries

China

Contacts

Public ContactYujie Zhao

The Seventh People's Hospital of Zhengzhou

lzyj74@126.com+86 18703677288

Outcome results

None listed

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