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RCVR (Residual CardioVascular Risk) Prospective Multicenter Study

RCVR (Residual CardioVascular Risk) Prospective Multicenter Study

Recruiting
20-90 years
All
Phase N/A

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Overview

The observational study aims to evaluate the long-term effects of residual cardiovascular risk on clinical outcomes following percutaneous coronary intervention (PCI). This risk includes thrombotic, metabolic, inflammatory, and procedural factors, which are assessed 1 month after the intervention. The primary question the study seeks to answer is:

What residual cardiovascular risk affects long-term clinical outcomes in patients undergoing PCI?

Participants will undergo artificial intelligence-based quantitative coronary analysis after PCI and will have comprehensive laboratory tests conducted at 1 month to evaluate residual cardiovascular risk, and then annually for 3 years post-intervention to assess changes in this risk.

Eligibility

Inclusion Criteria:

  • Patients who have undergone percutaneous coronary intervention.
  • Patients who have provided written informed consent.

Exclusion Criteria:

  • Under 19 years of age.
  • Pregnant, breastfeeding, or women of childbearing age.
  • Currently has a malignancy or has a history of malignancy within the past 5 years.
  • Life expectancy of less than 5 years.

Study details
    Coronary Artery Disease

NCT06619353

CHA University

7 September 2025

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FAQs

Learn more about clinical trials

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A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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