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Cardiac GSI Feasibility Study

Primary Purpose

High Risk of Significant Coronary Artery Disease

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Cardiac GSI
Sponsored by
University Hospital Plymouth NHS Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for High Risk of Significant Coronary Artery Disease focused on measuring CT coronary angiography, Coronary disease, Gemstone Spectral Imaging, Diagnostic value, Adaptive statistical iterative reconstruction, iterative reconstruction, Feasibility of coronary and myocardial assessment, novel Cardiac CT GSI protocol

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

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

Exclusion Criteria:

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

Sites / Locations

  • Plymouth Hospitals NHS Trust

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Anatomical accuracy Cardiac GSI vs ICA

Stress perfusion Cardiac GSI vs MPI-SPECT

Delayed enhancement Cardiac GSI vs CMR

Arm Description

The identification and quantification of coronary artery stenoses using Cardiac in comparison to ICA.

Assessment of the functional impact of coronary stenoses using Cardiac GSI in comparison to MPI-SPECT

Assessment of abnormal myocardial tissue characteristics representing ischaemic or scarred tissue using Cardiac GSI in comparison to CMR.

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

radiation burden of the Cardiac GSI techniques
The Discovery CT750 HD scanner uses a new image reconstruction technique called Adaptive Statistical Iterative Reconstruction (ASIR). ASIR uses more complex mathematical modelling for image reconstruction, thus reducing the need for statistical assumptions and reducing image noise and artefact. It also requires the less raw data and thus significantly less radiation dose. Studies suggest that using ASIR can achieve up to 40% dose reduction compared to Filtered Back Projection (FBP). However, the effect of ASIR and radiation dose reducing algorithms on image quality and accuracy has not been assessed and the difference in image quality and artefact suppression using the new technology remains to be established before its widespread dissemination into clinical practice.

Full Information

First Posted
February 28, 2013
Last Updated
October 21, 2016
Sponsor
University Hospital Plymouth NHS Trust
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1. Study Identification

Unique Protocol Identification Number
NCT01816750
Brief Title
Cardiac GSI Feasibility Study
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
October 2016
Overall Recruitment Status
Completed
Study Start Date
April 2013 (undefined)
Primary Completion Date
June 2016 (Actual)
Study Completion Date
June 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital Plymouth NHS Trust

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
High Risk of Significant Coronary Artery Disease
Keywords
CT coronary angiography, Coronary disease, Gemstone Spectral Imaging, Diagnostic value, Adaptive statistical iterative reconstruction, iterative reconstruction, Feasibility of coronary and myocardial assessment, novel Cardiac CT GSI protocol

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Non-Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Anatomical accuracy Cardiac GSI vs ICA
Arm Type
Experimental
Arm Description
The identification and quantification of coronary artery stenoses using Cardiac in comparison to ICA.
Arm Title
Stress perfusion Cardiac GSI vs MPI-SPECT
Arm Type
Experimental
Arm Description
Assessment of the functional impact of coronary stenoses using Cardiac GSI in comparison to MPI-SPECT
Arm Title
Delayed enhancement Cardiac GSI vs CMR
Arm Type
Experimental
Arm Description
Assessment of abnormal myocardial tissue characteristics representing ischaemic or scarred tissue using Cardiac GSI in comparison to CMR.
Intervention Type
Device
Intervention Name(s)
Cardiac GSI
Other Intervention Name(s)
Cardiac Gemstone Spectral Imaging
Intervention Description
A novel method of computed tomography scanning (Cardiac Gemstone Spectral Imaging - Cardiac GSI) and image reconstruction (Adaptive Statistical Iterative Reconstruction- ASIR.
Primary Outcome Measure Information:
Title
Feasibility - Assessment of rates of recruitment, acceptability of the procedure to patients, ease of CT acquisition
Description
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?
Time Frame
4 months
Secondary Outcome Measure Information:
Title
radiation burden of the Cardiac GSI techniques
Description
The Discovery CT750 HD scanner uses a new image reconstruction technique called Adaptive Statistical Iterative Reconstruction (ASIR). ASIR uses more complex mathematical modelling for image reconstruction, thus reducing the need for statistical assumptions and reducing image noise and artefact. It also requires the less raw data and thus significantly less radiation dose. Studies suggest that using ASIR can achieve up to 40% dose reduction compared to Filtered Back Projection (FBP). However, the effect of ASIR and radiation dose reducing algorithms on image quality and accuracy has not been assessed and the difference in image quality and artefact suppression using the new technology remains to be established before its widespread dissemination into clinical practice.
Time Frame
4 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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 Exclusion Criteria: 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ben Clayton, MBBS
Organizational Affiliation
Plymouth Hospitals NHS Trust (UK)
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Gareth Morgan-Hughes, MBBS
Organizational Affiliation
Plymouth Hospitals NHS Trust (UK)
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Franchesca Wotton, MBBS
Organizational Affiliation
Plymouth Hospitals NHS Trust (UK)
Official's Role
Study Director
Facility Information:
Facility Name
Plymouth Hospitals NHS Trust
City
Plymouth
State/Province
Devon
ZIP/Postal Code
PL6 8DH
Country
United Kingdom

12. IPD Sharing Statement

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