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NCT06619353

RCVR (Residual CardioVascular Risk) Prospective Study

Sponsor: CHA University

View on ClinicalTrials.gov

Summary

The goal of this observational study is to evaluate whether residual cardiovascular risk assessed at 1 month after percutaneous coronary intervention (PCI) is associated with long-term clinical outcomes in adult patients with coronary artery disease who are free from major adverse clinical events at 1 month after PCI. The main questions it aims to answer are: * Does residual cardiovascular risk at 1 month after PCI predict long-term net adverse clinical events? * Which components of residual cardiovascular risk are associated with subsequent adverse clinical outcomes? Participants will: * Undergo comprehensive laboratory testing at 1 month after PCI and annually thereafter. * Undergo artificial intelligence-based quantitative coronary angiographic analysis using DICOM datasets after PCI. * Be followed annually for up to 3 years after the 1-month assessment to evaluate clinical outcomes.

Official title: Residual CardioVascular Risk (RCVR) After Percutaneous Coronary Intervention: A Prospective Study

Key Details

Gender

All

Age Range

20 Years - 90 Years

Study Type

OBSERVATIONAL

Enrollment

500

Start Date

2024-06-17

Completion Date

2029-02

Last Updated

2026-02-18

Healthy Volunteers

No

Interventions

DIAGNOSTIC_TEST

Blood Sample

Patients' blood samples are tested at 1 month, and then annually for 3 years post-intervention to assess residual thrombotic, metabolic, and inflammatory risk.

OTHER

DICOM Dataset

Patients' DICOM dataset is evaluated using artificial intelligence-based quantitative coronary analysis to assess a procedural risk.

Locations (1)

CHA Bundang Medical Center

Seongnam-si, Gyeonggi-do, South Korea