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NCT03894423Active, not recruiting

Comprehensive Computed Tomography Guidance of Coronary Bypass Graft Surgery

Comprehensive CT Guided Coronary Bypass Graft Surgery

Source: ClinicalTrials.gov · Last updated 17 Apr 2026

Brief summary (registry, in English)

Apply CT angiography, CT perfusion imaging and advanced image processing techniques to improve revascularization decision-making and surgical strategies in patients undergoing coronary artery bypass graft surgery.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
22 Mar 2019
Start date
1 May 2019
Primary completion date
Dec 2026
Lead sponsor
Stanford University
NCT number
NCT03894423

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 1 May 2019 to the primary completion date, Dec 2026
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • 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.

Other illness

  • Technical feasibility of the cardiac CT exams: redo-CABG, significant arrhythmia/mal-conduction, congenital conditions, severe valvular disease or cardiomyopathy (to the extent that the CT acquisition is technically challenged), inadequate understanding of the English language (to provide consent or follow instructions during the exams).
  • 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.

Other

  • Inability to provide informed consent.

Who the study is looking for

  • Planned elective CABG for coronary artery disease.
  • CABG is the primary indication for surgery (but may include treatment of mild-moderate valvular disease).
  • Age: ≥40 years.

Age in the registry: 40 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Stanford University
Coordinator of this site? Confirm its status
Palo AltoUnited StatesUnknown status
Palo Alto Veterans Affaird Healthcare System
Coordinator of this site? Confirm its status
Palo AltoUnited StatesUnknown status
University of California San Diego
Coordinator of this site? Confirm its status
San DiegoUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.