Comprehensive Computed Tomography Guidance of Coronary Bypass Graft Surgery
NCT ID: NCT03894423
Last Updated: 2025-03-30
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
200 participants
OBSERVATIONAL
2019-05-01
2028-01-31
Brief Summary
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Detailed Description
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Aim 1: Predict restoration of myocardial perfusion from coronary artery bypass graft surgery. The investigators will perform cardiac CT before and after CABG and measure absolute changes in myocardial perfusion as the functional outcome of CABG. The investigators will investigate clinical, surgical and imaging variables in association with post-CABG perfusion improvement on a per-vessel and per-patient level.
Aim 2: Non-invasively quantify vessel-specific ischemia for meaningful CABG decisions.
The investigators will develop and validate tools for assessment of vessel-specific ischemia and viability. The investigators will assess the potential impact of CT guided CABG by comparing the per-vessel need for grafting with standard care.
Aim 3: Predict CABG benefit through multi-parameter flow simulations Hypothesis: Integration of myocardial perfusion and viability can improve flow simulation models to predict CABG outcome. The investigators will develop new computational fluid dynamics models enriched with functional parameters and explore the potential of virtual grafting to improve hemodynamic outcomes.
Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* CABG is the primary indication for surgery (but may include treatment of mild-moderate valvular disease).
* Age: ≥40 years.
Exclusion Criteria
* Overall safety: unstable clinical condition (clinical heart failure, unstable angina, myocardial infarction \<1 month prior).
* Radiation risk: pregnancy (cannot be ruled out), body weight \>100kg.
* CT contrast medium-related: known allergy, renal failure
* Vasodilator related: known allergy, bronchial asthma requiring daily use of bronchodilators, Mobitz II or 3rd degree AV block, sick sinus node disease, clinically significant carotid artery narrowing, severe aortic stenosis or LVOT narrowing, systolic blood pressure below 90mmHg, (continued) use of dipyridamole or aminophylline.
* Inability to provide informed consent.
40 Years
ALL
No
Sponsors
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National Heart, Lung, and Blood Institute (NHLBI)
NIH
University of California, San Diego
OTHER
VA Palo Alto Health Care System
FED
Stanford University
OTHER
Responsible Party
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Koen Nieman
Professor
Principal Investigators
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Koen Nieman, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Stanford University
Locations
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Palo Alto Veterans Affaird Healthcare System
Palo Alto, California, United States
Stanford University
Palo Alto, California, United States
University of California San Diego
San Diego, California, United States
Countries
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Central Contacts
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Facility Contacts
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Phyo Aung
Role: primary
Patricia Nguyen, MD
Role: backup
Koen Nieman, MD, PhD
Role: backup
Andrew Kahn, MD
Role: primary
Other Identifiers
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MZ-0048352
Identifier Type: OTHER
Identifier Source: secondary_id
IRB-49945
Identifier Type: -
Identifier Source: org_study_id
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