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Cardiac Risk Assessment Using Standard of Care Versus CTA and Heart Flow FFRct

Cardiac Risk Assessment Using Standard of Care Versus CTA and Heart Flow FFRct in Patients With End-Stage Liver Disease Under Consideration for Liver Transplant.

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04089969
Acronym
CRASCH-Liver
Enrollment
0
Registered
2019-09-16
Start date
2023-06-30
Completion date
2024-06-30
Last updated
2023-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Liver Failure, Coronary Artery Disease, Liver Transplant

Keywords

CTA, FFRct, CAD, End Stage Liver DIsease, Liver failure, Liver transplant

Brief summary

Coronary Artery Disease (CAD) is the narrowing or blockage of the artery of the heart and is prevalent in end-stage liver disease. Consultation with cardiologist and stress tests are recommended to patients under consideration for liver transplant. The purpose of this study is to evaluate if Computed Tomography Angiogram (CTA) and CTA-derived Fractional Flow Reserve (FFRct) procedure influences decisions about further cardiac testing compared with Standard of Care (SOC) such as consultation by a cardiologist, Echocardiogram (ultrasound of the heart), Electrocardiogram (ECG) and stress tests.

Detailed description

The purpose of this study is to determine in end-stage liver disease patients whether non-invasive assessment of coronary artery disease prior to liver transplant using CTA (CTA) and CTA-derived Fractional Flow Reserved (FFRct) is superior to current standard of care (SOC) cardiovascular evaluation such as formal consultation by a cardiologist, electrocardiogram, echocardiogram, and pharmacological stress test such (e.g. Dobutamine stress echocardiogram and lexiscan myocardial perfusion imaging). The investigational portion of this study is the CTA and FFRct, which is a special x-ray scan that can identify blockages in the arteries and determine if blood flow is impaired. The CTA and FFRct will be done within 2 weeks after the standard of care evaluation. All 100 patients will undergo standard of care stress test plus CTA/FFRct. The referring cardiologist will be blinded to the results of CTA/FFRct, and will make an initial recommendation based on the standard of care evaluation. After making the initial recommendation, the referring cardiologist will be unblinded to the CTA/FFRct results and make a final recommendation. The initial recommendation will consist of one of the following: further cardiac evaluation is not needed or cardiac catheterization is required. The final recommendation will consist of one of the following: further cardiac evaluation is not needed or cardiac catheterization is required. All patients will receive a 1 year phone follow up call. The hypothesis is that in End Stage Liver Disease (ESLD) patients, non-invasive assessment for CAD using CTA/FFRct is superior to SOC cardiovascular evaluation (stress etst, echocardiogram, ECG). This study will look at the frequency of how often CTA/FFRct changed the clinical recommendation compared with the standard of care alone (Initial recommendation versus final recommendation).

Interventions

DIAGNOSTIC_TESTCTA/FFRct

Computed Tomography Angiogram with Fractional Flow Reserve. A Ct scan of the heart's blood vessels.

DIAGNOSTIC_TESTSOC cardiovascular evaluation

Standard of care (SOC) cardiovascular evaluation i.e ECG, 2 D echocardiogram and pharmacologic stress test such as Dobutamine and Myocardial Perfusion Imaging stress test.

Sponsors

Corewell Health East
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SEQUENTIAL
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

Single-Blind decision-making study.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients with end-stage liver disease 2. Patients undergoing cardiovascular risk assessment prior to liver transplantation -

Exclusion criteria

1. Estimated Glomerular Filtration Rate (eGFR) \< 30 cc/min/1.73 m\^2 (unless patient is on dialysis or renal transplant is planned) 2. Heart rate \> 90 bpm despite beta blocker therapy 3. Body Mass Index (BMI) \> 40 plus chest obesity (i.e. truncal obesity and normal chest morphology is not an exclusion) 4. Pregnant Women

Design outcomes

Primary

MeasureTime frameDescription
Change in clinical recommendationwithin 2 weeks after SOC assessmentNumber of Participants whose clinical recommendation as initially determined by SOC assessment is changed following CTA/FFRct assessment.

Secondary

MeasureTime frameDescription
Frequency of detecting Coronary Artery Disease (CAD) by CTA/FFRctwithin 2 weeks after SOC assessmentNumber of Participants with agreement in CAD status detected by both Pharmacological stress test and also CTA/FFRct.
Cardiovascular morbidity1 yearNumber of participants with cardiovascular related Death, Myocardial Infarction (MI: defined as any 2 of following; 1. ischemic chest pain, 2. elevated troponin 3. pathologic Q waves or ischemic ST changes), or ischemia driven revascularization
Projected Health Care Costwithin 2 weeks after SOC assessmentDollar value of Standard of care treatment (related to CAD) and CTA/FFRct
Frequency of Detecting Myocardial Ischemia and the frequency of detecting the correct territory of the Myocardial Ischemia.within 2 weeks after SOC assessmentNumber of participants with Myocardial Ischemia and correct territory of Myocardial Ischemia detected by Pharmacological Stress Test vs CTA/FFRct

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026