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Clinical Trials in China / NCT07471763
Starting soon Observational

Prospective Lifespan Cohort of Myocardial Infarction

NCT07471763 · tracked via the Priya Life Science China tracker
Sponsor
Fujian Provincial Hospital
Phase
Observational
Started
2026-04-10
Last updated
2026-03-25

Condition(s) studied

Acute Myocardial Infarction (AMI)Stable AnginaUnstable Angina

Study summary

This prospective cohort study aims to establish a lifespan cohort of myocardial infarction and build a standardized, multidimensional, and shareable disease-specific database by systematically integrating clinical phenotypes, multi-omics data, and longitudinal follow-up information. Based on artificial intelligence and multi-omics integration, the study further seeks to develop a precision prevention and control framework for acute myocardial infarction covering the full continuum from early risk warning and accurate diagnosis to individualized treatment and long-term risk management.

The study will enroll adults aged 18 to 74 years, including two major populations: individuals at high risk of acute myocardial infarction, such as those with stable or unstable angina, and patients with confirmed acute myocardial infarction diagnosed according to the Fourth Universal Definition of Myocardial Infarction. Biospecimens, including venous blood, urine, and feces, will be collected, and participants will undergo standardized baseline assessment and follow-up.

The primary outcome is all-cause mortality during follow-up. Secondary outcomes include cardiovascular death, recurrent myocardial infarction, readmission due to heart failure, revascularization, stroke, stent thrombosis, and severe bleeding. This study is expected to provide scientific evidence and technical support for precision prevention, diagnosis, treatment, and long-term management of myocardial infarction.

Eligibility

Sex
ALL
Min age
18 Years
Max age
74 Years
Healthy volunteers
No
Inclusion Criteria: Age 18 to 74 years Diagnosed with stable angina, unstable angina, or acute myocardial infarction For acute myocardial infarction: symptom onset to hospital admission less than 24 hours, with patients undergoing emergency percutaneous coronary intervention prioritized Diagnosis of acute myocardial infarction according to the Fourth Universal Definition of Myocardial Infarction Willing to participate and able to provide written informed consent Able to complete baseline assessment, biospecimen collection, and long-term follow-up Exclusion Criteria: End-stage malignant tumor with expected survival of less than 1 year Severe hepatic or renal dysfunction (estimated glomerular filtration rate \<30 mL/min/1.73 m² or Child-Pugh class C) Active autoimmune disease or long-term use of immunosuppressive agents Pregnant or breastfeeding women Inability to provide informed consent or severe cognitive impairment Previous participation in another clinical study that may conflict with this project Any other condition considered by the investigators to make participation inappropriate

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Fuzhou University Affiliated Provincial Hospital Fuzhou Fujian

More Fujian Provincial Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07471763 on ClinicalTrials.gov ↗ ← All trials in China