Spontaneous Coronary Artery Dissection - AntipLatelet Therapy Intensity in Guided coNservative Management (SCAD-ALIGN) Trial
NCT07683923
ACS (Acute Coronary Syndrome), Acute Coronary Syndrome
Vancouver, British Columbia, Canada
View Trial DetailsNCT Number: NCT07128667
The incidence of acute myocardial infarction (AMI) in young patients is on the rise, placing a heavy health and economic burden on individuals, families, and society. The clinical phenotype and pathophysiological mechanisms of AMI in this population exhibit significant heterogeneity compared to elderly patients, and existing risk assessment tools have limited applicability in this specific group. The core problem this study aims to address is: how to accurately identify specific risk factors in young AMI patients and build an effective risk prediction model to prevent and optimize clinical diagnosis and treatment.
This study will adopt a prospective cohort design to collect multi-dimensional clinical data from young AMI patients. It will systematically analyze their clinical characteristics, risk factors, and coronary lesion status to comprehensively map the clinical, risk factor, and pathophysiological diversity of young AMI patients. Secondly, it will delve into identifying specific risk factors that influence the onset, progression, and long-term prognosis of young AMI. Thirdly, it will combine machine learning algorithms to develop a risk prediction model for young AMI, performing internal validation in the prospective cohort and external validation in the MIMIC-IV database. Simultaneously, it will explore novel biomarkers associated with disease onset and progression. The key outcomes of this study are to establish a high-quality clinical database of young AMI patients, design a risk prediction model for young AMI based on the study results, and produce high-level academic publications.
Trial opening soon.
Get Notified18 year–45 year
All sexes
Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Short-term endpoints (in-hospital and within 30 days post-discharge).Long-term endpoints (12 months post-discharge).
Time frame: Short-term endpoints (in-hospital and within 30 days post-discharge).Long-term endpoints (12 months post-discharge).
Time frame: Short-term endpoints (in-hospital and within 30 days post-discharge).Long-term endpoints (12 months post-discharge).
Contact information is provided by the study sponsor or research team.
China-Japan Friendship Hospital
Other
A Prospective Cohort Study on Clinical Characteristics, Risk Factors, and Long-Term Outcomes in Young Patients With Acute Myocardial Infarction
Acronym: AMI-Youth
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.
Published trials that share one or more normalized conditions with this study.
NCT07683923
ACS (Acute Coronary Syndrome), Acute Coronary Syndrome
Vancouver, British Columbia, Canada
View Trial DetailsNCT07685639
ACS (Acute Coronary Syndrome), Acute Coronary Syndrome
View Trial DetailsNCT07351643
ACS (Acute Coronary Syndrome), Acute Coronary Syndrome
Shenyang, Liaoning, China
View Trial DetailsNCT07264881
ACS (Acute Coronary Syndrome), Acute Coronary Syndrome
Beijing, Beijing Municipality, China
View Trial Details