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Completed

NCT Number: NCT01856504

Validation of an Intracycle CT Motion CORrection Algorithm for Diagnostic AccuracY

To demonstrate the incremental utility of SSF for individuals undergoing CCTA, with expected improvements in image quality and diagnostic accuracy.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Diagnostico Maipu, San Isidro, Argentina

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About this study

Hypothesis: Coronary CT angiography (CCTA) employing a novel intracycle motion compensation algorithm (SnapShot Freeze [SSF]) will be superior to CCTA without an intracycle motion compensation algorithm ("conventional" CCTA) for diagnostic accuracy and image quality.

Scientific Basis: Preliminary study (Leipsic, Min, Journal of Cardiovascular Computed Tomography [in press]) of coronary CT angiograms in individuals undergoing pre-procedural assessment for transcatheter aortic valve replacement (n=36) demonstrate improved image quality of CCTA using SSF compared to CCTA not using SSF. Importantly, individuals in this study did not receive heart rate slowing agents (e.g., beta blockers), and diagnostic image quality was substantially improved. While not statistically powered on a per-patient basis, per-segment diagnostic accuracy of CCTA using SSF was superior to conventional CCTA. These results are complementary to those derived from internal testing at GE Healthcare wherein phantom work has demonstrated improved diagnostic performance using SSF compared to conventional image acquisitions.

Long-term Goal/Purpose: To demonstrate the incremental utility of SSF for individuals undergoing CCTA, with expected improvements in image quality and diagnostic accuracy. If the aims of this study are achieved, the use of SSF for effective temporal resolution improvement may obviate (or reduce) the need for CT hardware for improved temporal resolution.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Consenting adult patients ≥18 years of age;
  • Suspected but without known prior history of CAD
  • Not actively taking heart rate lowering agents at least 48 hours prior to study (e.g., AV nodal blockers such as beta blockers, calcium channel blockers or digoxin)
  • Glomerular filtration rate >60 ml/min
  • CCTA and ICA within 1 week of each other with no interscan event (e.g., myocardial infarction or coronary revascularization)

Exclusion criteria

  • Incomplete ICA or CCTA;
  • Known CAD (prior myocardial infarction, PCI, CABG)
  • Atrial Fibrillation
  • Abnormal Renal Function (GFR <60 ml/min)
  • Unwilling or unable to give consent
  • Non-cardiac illness with life expectancy <1 year
  • Concomitant participation in another clinical trial in which subject is subject to investigational drug or device
  • Pregnant women
  • Allergy to iodinated contrast agent
  • Contraindications to nitroglycerin
  • Systolic blood pressure ≤90 mm Hg
  • Contraindications to β blockers or nitroglycerin

Treatment and study plan

Primary outcomes

  1. Diagnostic Accuracy

    Time frame: 30 days

    To compare the per-patient, per-vessel and per-segment diagnostic accuracy of CCTA with SSF to conventional CCTA, as compared to invasive quantitative coronary angiography.

  2. Diagnostic Interpretability

    Time frame: 30 days

    To compare the per-patient, per-vessel and per-segment diagnostic interpretability of CCTA with SSF to conventional CCTA, as compared to invasive quantitative coronary angiography.

  3. Image quality

    Time frame: 30 day

    To compare the per-patient, per-vessel and per-segment quantitative image quality of CCTA with SSF to conventional CCTA, as compared to invasive quantitative coronary angiography.

Secondary outcomes

  1. Upper threshold of heart rate

    Time frame: 1 day

    To determine the upper threshold of heart rate below which CCTA with SSF is most effective.

  2. incremental & additive value

    Time frame: 1 day

    To determine the incremental & additive value of SSF to conventional CCTA for diagnostic accuracy / diagnostic interpretability / image quality.

Sponsors and collaborators

Lead sponsor

MDDX LLC

Industry

Collaborators

  • GE Healthcare

Registry information

Official study title

Validation of an Intracycle CT Motion CORrection Algorithm for Diagnostic AccuracY: A Prospective Multicenter Study

Acronym: VICTORY

Important dates

Study start
2013
Primary completion
2015
Study completion
2015
First posted
May 17, 2013
Registry last updated
Apr 3, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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