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Patients who will be treated with a Cook CMD\n\nExclusion Criteria:\n\n1. Patients who declare they are unable to complete clinical follow-up visit at the time of enrollment, or\n2. Patients or his\u002Fher legally authorized representative objects to extraction of patient's data from the medical record, or unwilling to sign the Informed Consent.","ALL",{"count":203,"type":204},600,"ESTIMATED","OBSERVATIONAL","The purpose of this study is to evaluate the safety and performance of Cook's various Custom-Made Stent-graft Devices (CMD) used for endovascular treatment of the aorta and related diseases by collecting information on the real-world use of the devices.\n\nThe study results will be used to support the continuation of the CMDs on the market. 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