Complete Functional Assessment of Intermediate Coronary Artery Stenosis Before and After Transcatheter Aortic Valve Implantation (TAVI) in Patients With Severe Symptomatic Aortic Valve Stenosis

Who May Qualify: - Age \>18 years - Willing to participate and able to understand, read and sign the willing to sign a consent form document before the planned procedure - Severe symptomatic aortic stenosis with indication for TAVI according to current guidelines deemed by the Heart Team - Patients who have undergone coronary CT angiography before TAVI in which CAD could not be ruled out - CAD in one or more native major epicardial vessels or their branches by coronary angiogram with visually assessed coronary stenosis, in which the physiological severity of the lesion is in question (typically 40-90% diameter stenosis). - Eligible for invasive coronary angiography and functional assessment (FFR, RFR, CFR and IMR) - Eligible for coronary CT-angiography and functional assessment (CT-FFR) Who Should NOT Join This Trial: - Patients whose CT-angiography was determined to be non-diagnostic/unreadable during its evaluation - Previous coronary artery bypass grafting with patent grafts to the interrogated vessel - Patients with severe lesions with a diameter stenosis ≥ 90%, flow-limiting lesions, or a significant left main coronary artery stenosis - Critical coronary artery disease deemed by the Heart Team to require immediate revascularization - Contraindication to adenosine (e.g. bronchial asthma) - Chronic renal impairment with severe reduction of glomerular filtration rate (eGFR \<30 ml/min) - Presence of cardiogenic shock - Participation in another interventional study involving the left heart or coronary arteries Always talk to your doctor about whether this trial is right for you.