Fuzhou University Affiliated Provincial Hospital
Fuzhou, Fujian, 350001, China
NCT Number: NCT07471763
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.
Trial opening soon.
Get Notified18 year–74 year
All sexes
Observational
Fuzhou, Fujian, 350001, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
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
Time frame: From enrollment to the end of study follow-up, up to 5 years
Time frame: From enrollment to the end of study follow-up, up to 5 years
Time frame: From enrollment to the end of study follow-up, up to 5 years
Time frame: From enrollment to the end of study follow-up, up to 5 years
Time frame: From enrollment to the end of study follow-up, up to 5 years
Time frame: From enrollment to the end of study follow-up, up to 5 years
Time frame: From enrollment to the end of study follow-up, up to 5 years
Time frame: From enrollment to the end of study follow-up, up to 5 years
Contact information is provided by the study sponsor or research team.
Fujian Provincial Hospital
Other
A Prospective Lifespan Cohort Study of Myocardial Infarction for Building an Integrated Multidimensional Database and Developing an Artificial Intelligence- and Multi-omics-Driven Precision Prevention and Control System
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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