SMARTool: Collection of retrospective clinical and CCTA data and ethical approval of follow-up study (D1.1)

In the first Reporting Period M1-M6, the following specific objectives of SMARTool WP1 have been obtained: o Retrospective clinical and imaging data from the 540 patients participating to the FP7 EVINCI Study, for whom complete Follow-up data were available at December 2015, have been collected and analyzed. o Retrospective CCTA imaging data from the same EVINCI patients have been forwarded to FORTH and LUMC for quality assessment and testing of CCTA analyses. o An eligible population (N=358 patients from the EVINCI population and 38 patients from the FP7 ARTreat study population) has been selected according to the SMARTool study inclusion criteria. o SMARTool protocol, including updated CRFs for CCTA imaging acquisitions, has been submitted and approved at the Local Ethical Committee of the Clinical Coordination Centre in Pisa and distributed for submission to the Ethical Committees of the other clinical Centers. o A cloud image repository has been developed and populated with retrospective CCTA DICOM images datasets.