The Prognosis of Acute Myocardial Infarction

Completed

• Conditions: Acute Myocardial Infarction

• Registration Number: NCT02737956
• Lead Sponsor: Xinjiang Medical University

Brief Summary

This study aims to establish a registry and surveillance system for acute myocardial infarction (AMI) patients in Xinjiang, focusing on collecting comprehensive information including basic patient demographics, patient characteristics, diagnostic methods, treatment programs, and hospitalization outcomes such as mortality, treatment complications, hospitalization costs, and follow-up events (death, major adverse cardiac events). The goal is to identify and propose effective prevention strategies to reduce the incidence of AMI, optimize the management and outcomes of AMI patients by implementing guideline recommendations in clinical practice, and conduct analyses to develop effective treatment strategies and predictive models for clinical outcomes. This focus on Xinjiang aims to provide a comprehensive understanding of AMI within this specific geographic and demographic context, ultimately contributing to improved prevention, treatment, and management of AMI patients.

Detailed Description

The objective of this study is to establish a comprehensive registry and surveillance system for acute myocardial infarction (AMI) patients in Xinjiang. This platform is designed to support clinical research and translational medicine, aiming to improve the quality of AMI patient care through the integration of guideline recommendations into clinical practice. By collecting detailed information on patient demographics, characteristics, diagnostic methods, treatment programs, and outcomes, including mortality, complications, hospitalization costs, and follow-up events such as death and major adverse cardiac events, this study seeks to lay the foundation for future quality improvement initiatives and research. The ultimate goal is to translate research findings into improved care practices for AMI patients, thereby reducing morbidity and mortality associated with the condition. This endeavor will bridge the gap between clinical research and practical healthcare delivery, ensuring that advancements in the treatment and management of AMI directly benefit patients in Xinjiang, contributing to substantial improvements in healthcare outcomes.

Study Timeline

• Study Start: 2012-06-01
• Study First Submitted: 2016-04-05
• Study First Submitted QC: 2016-04-10
• Study First Posted: 2016-04-14
• Primary Completion: 2016-05-31
• Study Completion: 2023-12-10
• Status Verified: 2024-03
• Last Update Submitted: 2024-03-26
• Last Update Posted: 2024-03-28

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 7350

Inclusion Criteria

Acute myocardial infarction patients in hospitalized of the First Affiliated Hospital of Xinjiang Medical University (include diagnosed acute ST-elevation or non ST-elevation myocardial infarction).Diagnosis criteria must meet Universal Definition for AMI (2012).

Exclusion Criteria

1. Combined with severe valvular heart disease;
2. Combined with severe congenital heart disease;
3. Combined hyperthyroidism, anemia and other high-powered heart disease;
4. With pulmonary heart disease;
5. With hypertrophic obstructive cardiomyopathy;
6. Severe hypotension (SBP <90mmHg or DBP <60mmHg at enrollment);
7. Uncontrolled hypertension (SBP> 160 mmHg before PCI, and / or DBP> 100 mmHg);
8. Liver dysfunction (defined as ALT or total bilirubin is greater than the normal upper limit of 3 times);
9. Renal insufficiency (defined as serum creatinine greater than 1.5 times the normal upper limit);
10. High-risk bleeding patients, such as thrombocytopenia, blood diseases and other diseases;
11. active peptic ulcer and skin ulcers;
12. A patient who is allergic to clopidogrel, tegrellol, or aspirin;
13. Patients with a history of cardiogenic shock within two weeks;
14. pregnant and lactating women, during treatment can not be strict contraception of women of childbearing age;
15. In the past 3 months participated in other clinical researchers;
16. Persons who do not have legal or legal competence;
17. Any condition that the investigator considers unsuitable for participation in the clinical study.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Death	5 years	All-cause mortality, Cardiac mortality

Secondary Outcome Measures

Name	Time	Method
Major adverse cardiovascular events (MACE)	5 years	Cardiac death, non-fatal myocardial infarction, and target vessel revascularization.
stroke	5 years	ischemic stroke and hemorrhage
Major adverse cardiovascular and cerebrovascular events (MACCE)	5 years	Cardiac death, non-fatal myocardial infarction, target vessel revascularization and stroke.

Trial Locations

Locations (1)

First Affilliatted Hospital of Xinjiang Medical University; 🇨🇳 Ürümqi, Xinjiang, China