Clinical Trials Directory

Trials / Active Not Recruiting

Active Not RecruitingNCT06885619

Prediction of LVAR and MACE in AMI Though Plasma Multiomics Analysis

Prediction of Left Ventricular Adverse Remodeling and Major Adverse Cardiovascular Events in Patients With Acute Myocardial Infarction Though Plasma Multiomics Analysis

Status
Active Not Recruiting
Phase
Study type
Observational
Enrollment
1,000 (estimated)
Sponsor
Beijing Anzhen Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

To identify plasma multi-omics biomarkers that predict left ventricular adverse remodeling (LVAR) and major adverse cardiovascular events (MACE) in patients with acute myocardial infarction, and to investigate the molecular pathways linked to LVAR and MACE.

Detailed description

Despite advances in AMI treatment, a substantial proportion of patients develop LVAR, leading to heart failure and increased MACE risk. Conventional biomarkers (e.g., troponin, NT-proBNP) lack sufficient predictive power for adverse outcomes. Multi-omics approaches - integrating proteomics(e.g., exosome proteomics), metabolomics, transcriptomics and lipidomics - offer a systems-level view that may uncover novel prognostic signatures.

Conditions

Interventions

TypeNameDescription
OTHERDiagnostic Test: echocardiography and blood collectionBlood samples were collected from all patients at the time of myocardial infarction (MI) diagnosis. For those with acute ST-elevation myocardial infarction, blood samples were taken on the day of diagnosis(T0), as well as two days (T1), one week (T2) and one month (T3) after percutaneous coronary intervention (PCI). Echocardiography was performed at the time of STEMI diagnosis, and then again at one week, one month, and six months post-onset.

Timeline

Start date
2025-01-01
Primary completion
2027-12-31
Completion
2027-12-31
First posted
2025-03-20
Last updated
2025-07-31

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06885619. Inclusion in this directory is not an endorsement.