ClinicalTrials.Veeva

Menu

AI-Driven Dynamic Prediction of Non-Target Lesion Progression After PCI: A Chinese Multicenter Cohort Study (VISION-PCI)

C

China-Japan Friendship Hospital

Status

Enrolling

Conditions

Coronary Heart Disease (CHD)

Treatments

Other: percutaneous coronary intervention

Study type

Observational

Funder types

Other

Identifiers

NCT07312318
2025-NHLHCRF-PY-07

Details and patient eligibility

About

Coronary artery disease remains a leading cause of global mortality. Although percutaneous coronary intervention (PCI) improves patient outcomes, the long-term risk of major adverse cardiovascular events (MACE) driven by the progression of non-target lesions (NTLs) remains substantial and continues to increase, while current risk stratification tools remain inadequate for predicting NTL progression. This multicenter cohort study aims to develop an artificial intelligence (AI)-driven system for the dynamic prediction and precision stratification of NTL progression after PCI. Utilizing comprehensive multimodal data from 52,577 Chinese patients-including clinical profiles, multi-omics blood biomarkers, and coronary imaging-the research pursues three primary objectives: (1) to identify and validate 2-3 specific biomarkers for NTL progression risk using multi-omics approaches; (2) to construct an integrated risk assessment and early-warning system by applying machine learning to multimodal data for predicting NTL progression and MACE; and (3) to establish metabolic and imaging-based subtypes to create a precision management system that optimizes secondary prevention strategies by identifying specific high-risk populations. This study is expected to provide a novel tool for accurate identification of high-risk patients and personalized post-PCI management, ultimately aiming to improve long-term prognosis.

Enrollment

12,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Aged 18 years or older;
  2. Scheduled for or having undergone PCI;
  3. Baseline plasma sample obtainable;
  4. Informed consent obtained

Exclusion criteria

  1. Pregnancy or lactation;
  2. Severe hepatic or renal dysfunction;
  3. Active autoimmune disease;
  4. Missing critical data

Trial contacts and locations

1

Loading...

Central trial contact

Fang Wang

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems