Actively Recruiting

Age: 18Years +
All Genders
NCT06794684

PRogression of Atheroma Evaluated by CT Angiography and IntraCoronary Imaging tEchniques

Led by Ruijin Hospital · Updated on 2025-01-27

50000

Participants Needed

2

Research Sites

752 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a combined cohort study with retrospectively and prospectively enrolled coronary artery disease (CAD) patients. All the patients will undergo clinical follow-up for up to 5 years, and repeat coronary CTA will be conducted after 2 years. Comprehensive morphological and functional plaque analysis will be performed. The impact of these morphological and functional parameters, alongside cardiometabolic factors and pharmacological treatments on plaque progression and the occurrence of major adverse cardiovascular events (MACEs) will be analyzed. In addition, intracoronary imaging techniques will be used to improve the accuracy of plaque analysis by coronary CTA.

CONDITIONS

Official Title

PRogression of Atheroma Evaluated by CT Angiography and IntraCoronary Imaging tEchniques

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age ≥ 18 years
  • Clinically significant angina pectoris, or suspected CAD
  • Receive coronary CTA scan, with a visible plaque (defined as ≥25% diameter stenosis) in major coronary arteries.
Not Eligible

You will not qualify if you...

  • Unsuitable for coronary CTA (such as severe renal impairment, uncontrolled thyroid condition, allergic to iodine, etc.)
  • Receive percutaneous coronary intervention (PCI) within 6 months
  • Prior history of myocardial infarction or heart failure
  • Prior history of percutaneous coronary intervention (PCI) or coronary artery bypass graft (CABG)
  • Abnormal liver function (serum alanine aminotransferase [ALT] level exceeding 3 times the upper limit of normal) or abnormal kidney function (eGFR ≤30 ml/min)
  • Familial hypercholesterolemia
  • Estimated survival ≤ 1 year
  • Malignant tumor
  • Pregnant or lactation, or have the intention to give birth within one year
  • Poor coordinance, unable to follow-up

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

CAAC East China Aviation Personnel Medical Appraisal Center, Civil Aviation Shanghai Hospital

Shanghai, China, 200000

Actively Recruiting

2

Ruijin Hospital, Shanghai Jiaotong University School of Medicine

Shanghai, China, 200025

Actively Recruiting

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Research Team

X

Xiaoqun Wang

CONTACT

S

Shuo Feng

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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