Clinical Study of Cardiomyopeptidin on Postoperative Ischemia-reperfusion Injury in Patients With Primary PCI

NCT ID: NCT03958422

Last Updated: 2019-05-22

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE4
• Total Enrollment: 160 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-06-01
• Study Completion Date: 2020-01-31

Brief Summary

In this study, advanced techniques of myocardial nuclear magnetic perfusion scanning were used to quantitatively assess infarct size after acute myocardial infarction, saved viable myocardium, and microcirculatory obstruction area. Objectively and quantitatively evaluate early use of cardiomyopeptidin for direct PCI of ST-segment elevation myocardial infarction. After the improvement of microcirculation and increase the intervention effect of viable myocardium.

Detailed Description

This is a prospective, randomized, controlled, single-blind, single-center clinical trial. Patients with ST-segment elevation myocardial infarction (STEMI) who were admitted in the People's Liberation Army General Hospital were equally randomized to receive either cardiomyopeptidin or placebo, and patients in cardiomyopeptidin group are given the injection of cardiomyopeptidinl before primary percutaneous coronary intervention (PCI) and intravenous infusion of cardiomyopeptidin was performed 3 days after primary PCI. Myocardial perfusion flow grade was evaluated by the result of primary PCI. Myocardial infarct size, microvascular obstruction and salvage myocardium were evaluated by enhanced cardiac magnetic resonance (CMR). Major adverse cardiovascular events (nonfatal myocardial infarction, all-cause death, hospitalization for acute heart failure, and revascularization for angina) were observed during the 6-month follow-up. CMR is performed to evaluate the effect of cardiomyopeptidin before primary PCI on myocardial salvage and microcirculation perfusion in patients with STEMI.

Conditions

Survival Myocardial Area After Acute Myocardial Death; Left Ventricular Ejection Fraction

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Myocardin test group

Patients in cardiomyopeptidin group are given the injection of cardiomyopeptidinl before primary percutaneous coronary intervention (PCI) and intravenous infusion of cardiomyopeptidin was performed 3 days after primary PCI.

Group Type: EXPERIMENTAL

cardiomyopeptidin

Intervention Type: DRUG

The main component of cardiomyopeptidin is the peptide active substance extracted from the ventricular myocytes of healthy young pigs.

Blank test group

Patients in blank test group aren't given the injection of cardiomyopeptidinl before primary percutaneous coronary intervention (PCI) .

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

cardiomyopeptidin

The main component of cardiomyopeptidin is the peptide active substance extracted from the ventricular myocytes of healthy young pigs.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• 1) Sign the informed consent form;
• 2) Age ≥ 18 and ≤ 80 years old, gender is not limited;
• 3) Defining the diagnosis of acute myocardial infarction, with indications for direct coronary intervention;
• 4) Ischemic chest pain lasts for more than 30 minutes and adjacent ST or 2 leads of more than 2 or more leads (limb lead ≥ 0.1 mV, chest lead ≥ 0.2 mV) with or without elevated myocardial enzyme levels ;
• 5) The course of disease is ≤12 hours or accompanied by cardiogenic shock or heart failure (onset >12h).

Exclusion Criteria

• (1) Cardiogenic shock, Killip III-IV grade, papillary muscle rupture, interventricular septal perforation, ventricular ventricular fibrillation and electrical cardioversion, and III degree AVB implantation of temporary pacemaker before PCI;
• (2) LVEF ≤ 30%;
• (3) Previous history of PCI and CABG history;
• (4) acute and chronic infectious diseases (severe pneumonia, etc.);
• (5) Recent history of hemorrhagic stroke (within six months);
• (6) Combining liver and kidney dysfunction caused by various reasons;
• (7) History of valvular heart disease;
• (8) Congenital heart disease and pulmonary hypertension;
• (9) History of various types of cardiomyopathy;
• (10) bleeding and other thrombotic diseases;
• (11) severe anemia, thrombocytopenia and other blood system diseases;
• (12) Patients with malignant tumors, autoimmune diseases, and various causes of glucocorticoids and immunosuppressive agents;
• (13) Patients with a history of drug allergy, allergic diseases or allergies, or patients who are allergic to any of the ingredients in this product;
• (14) Patients with severe mental or neurological diseases;
• (15) pregnant women, lactating women, and subjects with a pregnancy plan during the trial;
• (16) According to the investigator's judgment, the subject is unable to complete the study or may not be able to comply (for administrative reasons or other reasons) the subjects required for this study.
• (17) Patients who have participated in other clinical trials in the past 3 months.Researchers believe that it is not appropriate to participate in this clinical trial.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Dalian Zhen-Ao Bio-Tech Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Yundai Chen

Role: STUDY_DIRECTOR

cardiology

Central Contacts

Geng Qian

Role: CONTACT

zouzouyuting@163.com

13810914587

Kai Yan

Role: CONTACT

ykanna_715@163.com

13940849959

Other Identifiers

DLZA2019P01

Identifier Type: -

Identifier Source: org_study_id