Skip to main content
TrialFinder
TrialFinder is for informational purposes only and does not provide medical advice. Always talk to your doctor about whether a trial is right for you.
RECRUITINGOBSERVATIONAL

Effect of Recombinant Human Brain Natriuretic Peptide on Ventricular Remodeling and Cardiac Function in Patients With Acute Anterior Myocardial Infraction Undergoing Percutaneous Coronary Intervention

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

This study is designed to evaluate the efficacy and safety of Recombinant Human Brain Natriuretic Peptide (rhBNP) in improving ventricular remodeling and cardiac function after acute anterior myocardial infarction undergoing percutaneous coronary intervention. 100 patients with acute anterior myocardial infarction after primary Percutaneous Coronary Intervention (pPCI) are randomly assigned 1:1 to rhBNP group(n=50) and control group(n=50) with follow-up of 24 weeks. Both groups are treated with standard therapy of AAMI, with the rhBNP group intravenous dripping rhBNP after pPCI for 3 days and the control group treated with placebo at the same time. The primary endpoint is the change in N terminal pro-B-type natriuretic peptide(NT-proBNP )and cardiac troponin T(cTnT) level.The secondary endpoint is the change in 24-week echocardiographic including left ventricle ejection fraction (LVEF) , left ventricular end-diastolic volume index (LVEDVI) and left ventricular end-systolic volume index (LVESVI), arrhythmia and cardiovascular events (death, cardiac arrest or cardiopulmonary resuscitation, hospitalization due to heart failure or angina pectoris).

Who May Be Eligible (Plain English)

Who May Qualify: 1. The first acute anterior myocardial infarction ( AMI ) within 12 hours ( or more than 12 hours but the ischemic symptoms continue ). 2. Age 18-75 years old, gender unlimited 3. Patients with acute anterior myocardial infarction undergoing emergency PCI within the effective time window 4. Successful reflow after interventional therapy ( TIMI = 3 ). 5. To understand and sign the willing to sign a consent form. Exclusion Criteria: 1. Patients with a history of coronary artery bypass grafting 2. Patients with cardiogenic shock 3. Patients with systolic blood pressure ( SBP ) ≤ 90 mmHg after treatment with vasopressors 4. Patients with mechanical complications ( ventricular septal perforation, mitral chordae rupture ) 5. Patients with suspected aortic dissection 6. Patients with severe liver and kidney dysfunction 7. Allergic or intolerant to rhBNP. 8. Patients with chronic renal insufficiency requiring long-term dialysis 9. Patients using diuretics during the screening period 10. Pregnant / lactating women 11. Heart diseases that are not suitable for vasodilators, such as severe valve stenosis, restrictive cardiomyopathy, restrictive pericarditis, etc Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: 1. The first acute anterior myocardial infarction ( AMI ) within 12 hours ( or more than 12 hours but the ischemic symptoms continue ). 2. Age 18-75 years old, gender unlimited 3. Patients with acute anterior myocardial infarction undergoing emergency PCI within the effective time window 4. Successful reflow after interventional therapy ( TIMI = 3 ). 5. To understand and sign the informed consent. Exclusion Criteria: 1. Patients with a history of coronary artery bypass grafting 2. Patients with cardiogenic shock 3. Patients with systolic blood pressure ( SBP ) ≤ 90 mmHg after treatment with vasopressors 4. Patients with mechanical complications ( ventricular septal perforation, mitral chordae rupture ) 5. Patients with suspected aortic dissection 6. Patients with severe liver and kidney dysfunction 7. Allergic or intolerant to rhBNP. 8. Patients with chronic renal insufficiency requiring long-term dialysis 9. Patients using diuretics during the screening period 10. Pregnant / lactating women 11. Heart diseases that are not suitable for vasodilators, such as severe valve stenosis, restrictive cardiomyopathy, restrictive pericarditis, etc

Treatments Being Tested

DRUG

Recombinant Human Brain Natriuretic Peptide

we divide our subjects into two groups;one is required to take recombinant human brain natriuretic peptide,the other is not required to take recombinant human brain natriuretic peptide

Locations (1)

the First Affiliated Hospital of Nanjing Medical University
Nanjing, Jiangsu, China