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临床试验/NCT06438393
NCT06438393尚未招募不适用

Screening Coronary Artery Disease Using artiFicial intelligencE in Non-contrast Computed Tomography

Universidade do Porto1 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2024年6月最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
1,000
试验地点
1
主要终点
Implement a machine learning model to discriminate patients with no CAD from patients with at least minimal disease (CAD-RADS=0 vs. CAD-RADS>0).

研究概览

简要总结

This project aims to improve direct patient care by reducing the risks of futile exposure to ionizing radiation and iodinated contrast in patients referred for coronary computed tomography angiography

详细描述

Since the last NICE guidelines update recommending computed tomography coronary angiography (CTCA) as the first line of investigation for patients with suspected coronary artery disease (CAD), there has been a high burden in the healthcare system and unnecessary exposition to radiation and iodine-containing contrast medium, especially in the youngest. Around 35% of patients who currently undergo CTCA have normal coronaries which means those patients were unnecessary exposed to radiation and contrast. A CTCA screening strategy to rule out CAD is needed to comply with the ALARA ("As Low As Reasonable Achievable") principles preventing radiation risks, reducing unnecessary scans and directing healthcare resources to those who will benefit from a CTCA.

We designed the SAFE-CT (Screening coronary Artery disease using artiFicial intelligencE in noncontrast Computed Tomography) study to develop a state-of-art artificial intelligence method to detect CAD as defined on CTCA using high-dimensional data (radiomics) extracted from the non-contrast cardiac computed tomography (CT). The model will be trained in 15,000 subjects scanned with paired non-contrast CT and CTCA and externally validated in an independent cohort of 1,000 subjects. In a preliminary analysis, non-contrast CT radiomics improved calcium score performance and discriminated CAD with an AUC of 0.91 (95% CI: 0.83-1.00). The algorithm will be converted into a user-friendly plugin to automatically decide whether the patient needs contrast. A real-world multicentre cohort study will be planned for software prospective validation and the creation of a large-scale proteomic biobank to support the translation of imaging biomarkers worldwide.

SAFE-CT can change the current CT scanning workflow by creating software that accurately rules out any CAD in >1/3 of patients referred for CTCA with low radiation and no contrast. This accurate machine learning model will be optimized to reach >90% sensitivity and negative predictive value and will bring several advantages for patients and the healthcare system:

  • Prevention of radiation and contrast exposition.
  • Increased CTCA scanning capacity for complex cases.
  • Widespread use of CT for CAD exclusion in the emergency department and in outpatient clinics of centres with no CTCA.
  • Improved screening tool for CAD in asymptomatic subjects.
  • Up- and downstream cost reduction.

The SAFE-CT project proposes a safer, low-cost, and personalized CTCA scanning strategy that fosters scientific and technological innovation with the potential to bring improvement to patient care and clinical practice, and, thereby, societal, and economic impact.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient with stable chest pain who underwent a CTCA

排除标准

  • Missing non-contrast CT image (coronary calcium score image)
  • Known coronary artery disease
  • Prior myocardial infarction
  • Prior PCI or CABG

结局指标

主要结局

Implement a machine learning model to discriminate patients with no CAD from patients with at least minimal disease (CAD-RADS=0 vs. CAD-RADS>0).

时间窗: 3 years

Create a national registry of cardiac CT

时间窗: 3 years

Build a non-contrast CT radiomic signature of CAD

时间窗: 3 years

Build a user-friendly plugin to facilitate users experience and distribution of our technology in clinical practice.

时间窗: 3 years

Implement a machine learning model to detect coronary inflammation as defined using the Fat Attenuation Index (FAI ≥ -70.1 HU) in patients with no visible coronary plaque (CAD-RADS=0).

时间窗: 3 years

Evaluate the real-world operationality and performance of the plugin in an international multicentre prospective cohort study.

时间窗: 3 years

次要结局

  • Setup a public CT imaging repository(3 years)
  • Setup a human blood biobank to identify the peripheral blood mononuclear cells (PBMCs) and plasma proteomics associated with CT data and clinical outcomes.(3 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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