A stent graft (GORE® Ascending Stent Graft) to repair ascending aorta lesions in people at high surgical risk

You may qualify if

• ASG Device Alone Arm The patient is/has: Ascending Aortic pathologies warranting surgical repair compatible with the treatment requirements of the ASG device meeting any of the following criteria: Aneurysm; Fusiform aneurysm (≥50mm or documented growth rate >0.5cm/year); Saccular aneurysm (no diameter criteria); Pseudoaneurysms (>30 days post-surgery, no diameter criteria) Non-aneurysm; Penetrating Aortic Ulcers (PAUs) (no diameter criteria); Pseudoaneurysms, following open surgical repair of a Type A dissection (>30 days post-surgery, no diameter criteria)
• Anatomic compatibility with ASG device based on Gore Imaging Sciences review.; Treatment must be limited to the ascending aorta; Lesion location is ≥2cm distal to the most distal coronary artery ostia; Distal extent of the lesion is located ≥2cm proximal to the origin of the Brachiocephalic Artery (BCA); Proximal and distal landing zones must be ≥2cm in length; Landing zones cannot be heavily calcified, or heavily thrombosed; Landing zone diameter between 27mm - 48mm; For patients with prior replacement of the ascending aorta and/or aortic arch by an endovascular or surgical graft, there must be at least ≥2 cm overlap of ASG device and previously implanted graft.
• Considered high-risk for open surgical repair by meeting any of the following criteria:; ≥75 years of age; Previous median sternotomy; Documented identification of other subject-specific risk factors (e.g., medical history, active medical diagnosis) by a study investigator and an experienced open ascending and/or aortic arch surgeon (e.g., cardiothoracic surgeon).
• Age ≥18 years at time of informed consent signature
• Adequate vascular access via transfemoral or retroperitoneal approach
• Informed Consent Form (ICF) signed by the subject or legally authorized representative
• Agrees to comply with protocol requirements, including imaging and 5-year follow-up
• ASG + TBE Device Arm The patient is/has: Ascending and/or Arch Aortic pathologies warranting surgical repair compatible with the treatment requirements of the ASG device and meeting any of the following criteria: Aneurysms; Fusiform aneurysm (≥55 mm or documented growth rate >0.5cm/year); Saccular aneurysm (no diameter criteria); Pseudoaneurysms (>30 days post-surgery, no diameter criteria) Non-aneurysms; Penetrating Aortic Ulcers (no diameter criteria); Pseudoaneurysms, following open surgical repair of a Type A dissection (>30 days post-surgery, no diameter criteria); Chronic de novo (>90 days) Type A aortic dissection requiring treatment; Chronic de novo aortic dissection with primary entry tear in the ascending aorta or arch; Chronic de novo aortic dissection with primary entry tear in the descending thoracic aorta with retrograde involvement of the aortic arch and/or ascending aorta; Residual aortic dissection following surgical repair of Type A aortic dissection requiring treatment (>30 days post-surgery)
• Anatomic compatibility with ASG device used in combination with the TBE Device based on Gore Imaging Sciences review. Proximal Aortic Landing Zone:; Landing zone is native aorta or surgical graft; Lesion location is ≥2cm distal to the most distal coronary artery ostia; Proximal landing zone must be ≥2cm in the ascending aorta.; Landing zone cannot be aneurysmal, heavily calcified, or heavily thrombosed; Landing zone diameter between 27mm - 48mm; Acceptable proximal landing zone outer curvature length for the required device Branch Vessel Landing Zone:; Length of ≥2.5 cm proximal to first major branch vessel; Target branch vessel inner diameters of 11-18 mm; Target branch vessel landing zone must be in native vessel that cannot be heavily calcified, or heavily thrombosed Distal Aortic Landing Zone:; Outer curvature must be ≥2 cm proximal to the celiac artery; Aortic inner diameters between 16-42 mm; Landing zone in native aorta or previously implanted GORE® TAG® Conformable Thoracic Stent Graft (CTAG Device)
• Considered high-risk for open surgical repair by meeting any of the following criteria:; ≥75 years of age; Previous median sternotomy; Documented identification of other subject-specific risk factors (e.g., medical history, active medical diagnosis) by a study investigator and an experienced open ascending and/or aortic arch surgeon (e.g., cardiothoracic surgeon).
• Age ≥18 years at time of informed consent signature
• Adequate vascular access via transfemoral or retroperitoneal approach
• Informed Consent Form (ICF) signed by the subject or legally authorized representative
• Agrees to comply with protocol requirements, including imaging and 5-year follow-up
• Surgical Follow-up Cohort Subjects who meet the following criteria will be followed:; The aortic lesion involves the ascending aorta and/or aortic arch; The subject is determined to be high-risk for open surgical repair per the protocol requirements; The subject is at least 18 years of age; The subject is willing to comply with the protocol requirements; Open surgery to repair the aortic lesion the patient was screened for is intended to be performed at the investigational site responsible for initiating the screening process for the study

You can't join if

• ASG Device Alone Arm The patient is/has: De novo Type A dissection
• Requires immediate treatment
• Dissected great vessels requiring treatment
• Anticipated need for coronary or aortic valve intervention within one year post treatment
• Any aortic valve repair or replacement including transcatheter aortic valve replacement (TAVR) or coronary artery intervention within 30 days prior to treatment
• Complex percutaneous coronary intervention (PCI) or treatment for acute coronary syndrome requiring Dual Anti Platelet Therapy (DAPT) within 30 days prior to treatment
• Open chest surgical repair within 30 days prior to treatment
• Presence of Intramural Hematoma (IMH) in landing zones
• Prosthetic heart valve in the aortic position that precludes safe delivery of the ASG device
• Aortic insufficiency grade 3 or greater
• Previous endovascular repair with a non-Gore device that would interfere with or result in contact with planned repair
• Concomitant vascular disease requiring treatment that is not planned for index endovascular procedure
• Any stroke or myocardial infarction within 6 weeks prior to treatment
• Presence of protruding and/or irregular thrombus and/or atheroma in the ascending aorta or aortic arch or any other factors that could increase the risk of stroke based on imaging review
• Known degenerative connective tissue disease (e.g., Marfan's or Ehler-Danlos Syndrome, EDS)
• Participation in investigational drug or medical device study within one year of enrollment unless approved by the sponsor
• Known history of drug abuse within one year of treatment
• Pregnant at time of procedure
• Active infected aorta, mycotic aneurysm
• Active systemic infection (e.g., infection requiring treatment with parenteral anti-infective medication)
• Renal failure, defined as patients with an estimated Glomerular Filtration Rate (eGFR) <30 (mL/min/1.73 m2) or currently requiring dialysis
• Life expectancy <12 months
• Known sensitivities or allergies to the device materials
• Known hypersensitivity or contraindication to anticoagulants or contrast media, which is not amenable to pre-treatment
• Body habitus or other medical condition which prevents adequate fluoroscopic and CT visualization of the aorta
• ASG + TBE Device Arm The patient is/has: Acute and subacute de novo Type A dissection (defined as <90 days)
• Requires immediate treatment
• Dissected great vessels requiring treatment
• Anticipated need for coronary or aortic valve intervention within one year post treatment
• Any aortic valve repair or replacement including transcatheter aortic valve replacement (TAVR) or coronary artery intervention within 30 days prior to treatment
• Complex percutaneous coronary intervention (PCI) or treatment for acute coronary syndrome requiring Dual Anti Platelet Therapy (DAPT) within 30 days prior to treatment.
• Open chest surgical repair within 30 days prior to treatment
• Presence of Intramural Hematoma (IMH) in landing zones
• Prosthetic heart valve in the aortic position that precludes safe delivery of the ASG device
• Aortic insufficiency grade 3 or greater.
• Previous endovascular repair with a non-Gore device that would interfere with or result in contact with planned repair
• Concomitant vascular disease requiring treatment that is not planned for index endovascular procedure
• Any stroke or myocardial infarction within 6 weeks prior to treatment
• Presence of protruding and/or irregular thrombus and/or atheroma in the ascending aorta or aortic arch or any other factors that could increase the risk of stroke based on imaging review
• Known degenerative connective tissue disease (e.g., Marfan Syndrome or Ehlers-Danlos Syndrome, EDS)
• Participation in investigational drug or medical device study within one year of enrollment unless approved by the sponsor
• Known history of drug abuse within one year of treatment
• Pregnant at time of procedure
• Active infected aorta, mycotic aneurysm
• Active systemic infection (e.g., infection requiring treatment with parenteral anti-infective medication)
• Renal failure, defined as patients with an estimated Glomerular Filtration Rate (eGFR) <30 (mL/min/1.73 m2) or currently requiring dialysis
• Life expectancy <12 months
• Known sensitivities or allergies to the device materials
• Known hypersensitivity or contraindication to anticoagulants or contrast media, which is not amenable to pre-treatment
• Body habitus or other medical condition which prevents adequate fluoroscopic and CT visualization of the aorta
• Previous instance of Heparin Induced Thrombocytopenia type 2 (HIT-2) or known hypersensitivity to heparin or a history of a hypercoagulability disorder and/or state