Computed TomogRaphic Evaluation of Atherosclerotic DEtermiNants of Myocardial IsChEmia
Status: | Active, not recruiting |
---|---|
Conditions: | Angina, Peripheral Vascular Disease, Cardiology |
Therapuetic Areas: | Cardiology / Vascular Diseases |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 2/17/2019 |
Start Date: | May 2014 |
End Date: | December 31, 2020 |
Computed TomogRaphic Evaluation of Atherosclerotic DEtermiNants of Myocardial IsChEmia (The CREDENCE Trial)
The study seeks to determine the accuracy of using anatomic and physiologic information
measurable by computed tomography features of stenosis, plaque, fractional flow reserve-CT
and to compare this measure to stress testing for the detection of myocardial ischemia
against the gold standard of cardiac catheterization with fractional flow reserve. The
hypothesis of this proposal is that integrating anatomic plaque features with physiologic
fractional flow reserve-CT will optimize identification of coronary lesions that are
ischemia-causing by computed tomography .
measurable by computed tomography features of stenosis, plaque, fractional flow reserve-CT
and to compare this measure to stress testing for the detection of myocardial ischemia
against the gold standard of cardiac catheterization with fractional flow reserve. The
hypothesis of this proposal is that integrating anatomic plaque features with physiologic
fractional flow reserve-CT will optimize identification of coronary lesions that are
ischemia-causing by computed tomography .
The CREDENCE trial will be a prospective multicenter cross-sectional study of 618 individuals
(n=309 [derivation cohort]; n=309 [validation cohort]) who will undergo stress test, computed
tomography, cardiac catheterization and fractional flow reserve. For the purposes of the
study, either stress test or computed tomography will have been performed for clinical
purposes, with the other test being performed as part of trial procedure. Study analyses will
focus on the diagnostic performance of the information derived by stress test versus computed
tomography against an invasive gold standard of cardiac catheterization and fractional flow
reserve for an endpoint of vessel territory-specific ischemia. In keeping with prior studies,
vessel territories will be comprised of the left anterior descending artery (and diagonal
branches), the left circumflex artery (and obtuse marginal branches) and the right coronary
artery (and posterolateral branch and posterior descending artery).
To date, the relative performance of traditional stress imaging testing compared to the
entirety of information proffered by CT has not been assessed compared to an unbiased gold
standard. The study proposed herein will directly address this unmet need.
(n=309 [derivation cohort]; n=309 [validation cohort]) who will undergo stress test, computed
tomography, cardiac catheterization and fractional flow reserve. For the purposes of the
study, either stress test or computed tomography will have been performed for clinical
purposes, with the other test being performed as part of trial procedure. Study analyses will
focus on the diagnostic performance of the information derived by stress test versus computed
tomography against an invasive gold standard of cardiac catheterization and fractional flow
reserve for an endpoint of vessel territory-specific ischemia. In keeping with prior studies,
vessel territories will be comprised of the left anterior descending artery (and diagonal
branches), the left circumflex artery (and obtuse marginal branches) and the right coronary
artery (and posterolateral branch and posterior descending artery).
To date, the relative performance of traditional stress imaging testing compared to the
entirety of information proffered by CT has not been assessed compared to an unbiased gold
standard. The study proposed herein will directly address this unmet need.
Inclusion Criteria:
1. Age >18 years
2. Scheduled to undergo clinically-indicated non-emergent invasive coronary angiography
Exclusion Criteria:
1. Known CAD (myocardial infarction [MI], percutaneous coronary interventions [PCIs],
coronary artery bypass graft [CABG],)
2. Hemodynamic instability
3. Inability to provide written informed consent
4. Concomitant participation in another clinical trial in which subject is subject to
investigational drug or device
5. Pregnant state
6. Absolute contraindication to iodinated contrast due to prior near-fatal anaphylactoid
reaction (laryngospasm, bronchospasm, cardiorespiratory collapse, or equivalent)
7. Serum creatinine ≥1.7 mg/dl or Glomerular Filtration Rate <30 ml/min
8. Baseline irregular heart rhythm (e.g., atrial fibrillation, etc.)
9. Heart rate ≥100 beats per minute
10. Systolic blood pressure ≤90 mm Hg
11. Contraindications to β blockers or nitroglycerin or adenosine
12. BMI >40 kg/m2
We found this trial at
11
sites
Vancouver, British Columbia V6T 1W5
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171 Ashley Avenue
Charleston, South Carolina 29425
Charleston, South Carolina 29425
843-792-1414
Phone: 843-876-7146
Medical University of South Carolina The Medical University of South Carolina (MUSC) has grown from...
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Houston Methodist Hospital Houston Methodist is comprised of a leading academic medical center in the...
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