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临床试验/NCT01816750
NCT01816750已完成不适用

Pilot Study to Assess the Feasibility and Diagnostic Performance of Computed Tomographic Coronary Angiography Using Cardiac Gemstone Spectral Imaging (Cardiac GSI) in Patients With High-risk of Significant Coronary Artery Disease and Myocardial Scar

University Hospital Plymouth NHS Trust2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2013年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
60
试验地点
2
主要终点
Feasibility - Assessment of rates of recruitment, acceptability of the procedure to patients, ease of CT acquisition

研究概览

简要总结

The recently introduced Computed tomography (CT) scanner, Discovery CT750 HD (GE Healthcare, Milwaukee), incorporates a battery of innovations aimed at improving diagnostic image quality, evaluating perfusion and assessing for scar, in an effort to address the current shortcomings of Computed tomographic coronary angiography (CTCA) in patients with significant coronary artery disease. The new scanner will use a novel method of scanning (Cardiac Gemstone Spectral Imaging - Cardiac GSI) and image reconstruction (Adaptive Statistical Iterative Reconstruction- ASIR) as opposed to standard definition 64-slice CT Multi-detector row computed tomography(MDCT)and Filtered Back Projection (FBP) used by the conventional CT scanners. The Cardiac GSI protocol enables the scanner to acquire images at two different x-ray energies almost simultaneously, which can be post-processed to selectively reduce beam hardening artefacts and delete materials with specific attenuating properties from the images, such as coronary calcium. ASIR offsets the potential increase in radiation dose required for Cardiac GSI scanning. This will potentially result in images of higher diagnostic quality with an equivalent or perhaps lower dose of radiation compared to present technology.

Furthermore, it is hypothesised that dual-energy acquisition may improve the accuracy of the assessment of perfusion.

Although initial in-vitro results are encouraging, this technology has not been rigorously assessed with regards to its feasibility and diagnostic quality, limiting its applicability in routine clinical practice. This assessment will require a trial comparing the accuracy of Cardiac GSI CTCA with that of Invasive coronary angiography (ICA) for anatomical assessment of stenosis, Myocardial Perfusion Imaging with Single Photon Emission Computed Tomography (MPI-SPECT) for assessment of perfusion and Cardiac Magnetic Resonance (CMR) for assessment of myocardial scar. We have designed a pilot study in this regard which will help us assess the feasibility of the scan protocol and provide data to power a larger study to assess the diagnostic remit of Cardiac GSI scanning in the assessment of patients with high-risk of significant coronary artery disease and myocardial scar.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • Accuracy arm
  • Patients >50 years of age
  • Suspected or known coronary artery disease referred for ICA
  • Stress perfusion arm
  • Patients >50 years of age
  • Suspected or established coronary artery disease referred for MPI-SPECT for assessment of inducible ischaemia
  • Delayed enhancement arm
  • Patients >50 years of age
  • Referred for CMR for assessment of myocardial viability/scar

排除标准

  • Accuracy arm
  • Consent cannot be obtained
  • Patient BMI > 30 kg /m2
  • NYHA class III or IV heart failure
  • Chronic total occlusion of target epicardial coronary artery
  • Urgent revascularisation required
  • Allergy to iodinated contrast or previous contrast induced nephropathy
  • Intolerance or contraindication to beta-blockers
  • Uncontrolled heart rhythm disturbances
  • 2nd or 3rd degree atrioventricular block
  • Estimated glomerular filtration rate <30ml/min within two weeks prior to procedure or chronic renal failure on dialysis
  • Pregnancy
  • Stress perfusion arm
  • As above, plus:
  • Asthma (any) or intolerance to adenosine
  • Delayed enhancement arm
  • As for Accuracy arm

结局指标

主要结局

Feasibility - Assessment of rates of recruitment, acceptability of the procedure to patients, ease of CT acquisition

时间窗: 4 months

Assessment of rates of recruitment, acceptability of the procedure to patients, ease of CT acquisition. This pilot study will add to this assessment with specific information about the diagnostic performance of the novel scanning technique: * Are images of sufficient quality to be diagnostic? * Is diagnosis likely to be non-inferior to current comparable techniques, sufficient to justify a formal study?

次要结局

  • radiation burden of the Cardiac GSI techniques(4 months)

研究者

发起方
University Hospital Plymouth NHS Trust
申办方类型
Other
责任方
Sponsor

研究点 (2)

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