Clinical trial Recruiting at 1 site Observational Ages 40 to 70

How coronary artery shape affects plaque and blood flow

Official title: High-Risk Plaques Identification Using Coronary Computed Tomography and Computational Fluid Dynamics

Run by Bangladesh University of Engineering and Technology · NCT07002697 · Data updated 2026-11-12

This project tests whether combining coronary CT scans with computer simulations of blood flow can help identify high-risk plaques in adults aged 40–70 who have symptoms or risk factors for coronary artery disease.

Quick facts

Study typeObservational
Ages40 Years to 70 Years
SexAll
Enrollment30 (estimated)
SponsorBangladesh University of Engineering and Technology
Academic / other
Drugs / interventionsradiation
Locations1 site (Dhaka)
StatusRecruiting
StartedAugust 10, 2024
Main results expectedOctober 11, 2025
Study endsApril 11, 2026
Registry record updatedJune 3, 2025
Trial IDNCT07002697 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 40–70 years old with chest pain or multiple coronary risk factors who can undergo contrast CT and provide informed consent are ideal candidates.

Probably not a fit

People with severe renal impairment, prior allergic reaction to iodinated contrast, or who are pregnant or breastfeeding are unlikely to be eligible or to benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational project combines coronary CT imaging (CCT) with computational fluid dynamics (CFD) to map blood flow patterns around atherosclerotic plaques. Adults with symptoms or multiple coronary risk factors undergo gated multi-detector CCT with iodinated contrast, followed by image reconstruction and CFD simulation using Mimics and Ansys software. The workflow includes patient selection, image segmentation, CFD modeling, and analysis of plaque features such as positive remodeling, low attenuation, and napkin-ring sign. The goal is to link plaque morphology and local hemodynamics to improve non-invasive prediction of lesions likely to cause acute coronary syndrome.

Why it matters

Potential benefit: If successful, this could help doctors identify plaques likely to cause heart attacks earlier and guide targeted preventive treatment.

How similar studies have gone: Related approaches like CT-derived FFR and CFD analyses of plaque hemodynamics have shown promising results, but integrating detailed plaque features with CFD for ACS prediction is still relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adults aged 40-70 years.
* Presenting with symptoms of CAD (e.g., chest pain, shortness of breath) or having multiple risk factors (e.g., hypertension, diabetes, smoking).
* Able to provide informed consent.

Exclusion Criteria:

* Severe renal impairment (due to contrast media risk).
* Previous allergic reaction to iodinated contrast media.
* Pregnant or lactating women.

Where it's running

  • National Institute of Cardiovascular Disease (NICVD)
    Dhaka, Bangladesh
    Recruiting

Study contacts

  • Principal investigator: Muhammad Tarik Arafat, PhD — Department of Biomedical Engineering, Bangladesh University of Engineering and Technology (BUET), Dhaka - 1205
  • Study coordinator: Muhammad Tarik Arafat, PhD
  • Email: tarikarafat@bme.buet.ac.bd
  • Phone: 01911764467

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.