The PLATFORM Study: Prospective LongitudinAl Trial of FFRct: Outcome and Resource IMpacts)

The OVERALL OBJECTVE of this post-market, multicenter, longitudinal, prospective,
consecutive cohort study is to compare clinical outcomes, resource utilization, and quality
of life (QOL) in subjects receiving standard practice evaluation and treatment versus
subjects receiving FFRCT-guided evaluation and treatment in subjects with suspected CAD in
order to further inform patients, health care providers, and other stakeholders about which
technologies are most effective and efficient in the diagnosis of CAD. Cohort 1 of this
study will assess outcomes incorporating standard practice evaluation and Cohort 2 will
assess outcomes incorporating FFRCT-guided evaluation. Each Cohort will be further
delineated based upon initial presentation, whereas subjects presenting for initial
non-invasive testing will be designated as Cohorts 1A and 2A; and subjects already referred
for ICA will be designated as Cohorts 1B and 2B.

SPECIFIC OBJECTIVES for sequential cohort comparisons:

1. To compare the rate of ICA documenting non-obstructive coronary artery disease,
clinical outcomes, and QOL following standard practice for diagnostic and treatment
planning modalities in Cohort 1 versus incorporating FFRCT as the preferred test to
guide further invasive management and medical treatment in Cohort 2;

2. To compare resource utilization following standard practice for diagnostic and
treatment pathways in Cohort 1 versus incorporating FFRCT as the preferred test to
guide further invasive management and medical treatment in Cohort 2;

3. To provide supporting data for generating new guidelines for diagnosis and prognosis of
CAD with comparative analysis of the risk stratification with the Updated
Diamond-Forrester risk model (UDF);

4. To provide society including patients, health care providers and other stakeholders
with information about which diagnostic technologies are most effective and efficient
in managing patients with CAD.

Inclusion Criteria:

- Age >18 years

- Providing written informed consent

- Subjects with intermediate likelihood of obstructive CAD with an Updated
Diamond-Forrester (UDF) risk score 20-80% with symptomatic, suspected CAD who:

- In Cohort 1A & 2A only are scheduled to undergo initial clinically-indicated
non-invasive coronary evaluation, and have not undergone non-invasive coronary
evaluation, including exercise tolerance testing, stress echocardiography, SPECT or
MRI, or cCTA, within the past 90 days OR ICA at any time; or

- In Cohort 1B & 2B only have been referred to invasive coronary angiography (ICA) and
have not undergone ICA within the past 90 days

- Ability to undergo cCTA

Exclusion Criteria:

- Suspicion of acute coronary syndrome. Subjects experiencing unstable angina are not
excluded where clinical documentation has ruled out a myocardial infarction.

- Prior, clinically documented myocardial infarction

- PCI prior to first test

- CABG prior to first test

- Contraindications for cCTA such as:

- Presence of pacemaker or internal defibrillator leads

- Atrial Fibrillation

- Known anaphylactic allergy to iodinated contrast

- Pregnancy or unknown pregnancy status in women of childbearing potential

- Body mass index >35 kg/m2

- Contraindication to acute beta blockade

- Contraindication to acute sublingual nitrate administration

- Prosthetic heart valve

- Contraindications to FFRCT

- Complex Congenital Heart disease other than anomalous coronary origins alone

- Ventricular septal defect with known Qp/Qs>1.4

- Requiring an emergent procedure within 48 hours of presentation

- Evidence of active clinical instability, including cardiogenic shock, unstable blood
pressure with systolic blood pressure <90 mmHg, or NYHA Grade III or IV congestive
heart failure or acute pulmonary edema

- Any active, serious, life-threatening disease with a life expectancy of less than 2
years

- Inability to comply with study follow-up requirements

- Current participation in any other clinical trial involving an investigational device
or dictating care pathways at the time of enrollment.