Portico Re-sheathable Transcatheter Aortic Valve System US IDE Trial

Trial details

Who runs it

Abbott Medical Devices

Trial code

NCT02000115

Record updated

20 July 2025

Original description

The objective of the PORTICO pivotal IDE trial is to evaluate the safety and effectiveness of the St Jude Medical (SJM) Portico Transcatheter Heart Valve and Delivery Systems (Portico) in the treatment of severe symptomatic aortic stenosis via transfemoral and alternative delivery methods in high risk and extreme risk patients.Read full original descriptionShow less

The objective of the PORTICO pivotal IDE trial is to evaluate the safety and effectiveness of the St Jude Medical (SJM) Portico Transcatheter Heart Valve and Delivery Systems (Portico) in the treatment of severe symptomatic aortic stenosis via transfemoral and alternative delivery methods in high risk and extreme risk patients.

Inclusion: Subjects must have co-morbidities such that the surgeon and cardiologist Co-Investigators concur that the predicted risk of operative mortality is ≥15% or a minimum Society of Thoracic Surgeons (STS) score of 8%. A candidate who does not meet the STS score criteria of ≥ 8% can be included in the study if a peer review by at least two surgeons concludes and documents that the patient's predicted risk of operative mortality is ≥15%. The surgeon's assessment of operative comorbidities not captured by the STS score must be documented in the study case report form as well as in the patient medical record; Subject is 21 years of age or older at the time of consent; Subject has senile degenerative aortic valve stenosis with echocardiographically derived criteria: mean gradient >40 mmHg or jet velocity greater than 4.0 m/s or Doppler Velocity Index <0.25 and an initial aortic valve area (AVA) of ≤ 1.0 cm2 (indexed effective orifice area (EOA) ≤ 0.6 cm2/m2). (Qualifying AVA baseline measurement must be within 60 days prior to informed consent); Subject has symptomatic aortic stenosis as demonstrated by New York Heart Association (NYHA) Functional Classification of II, III, or IV; The subject has been informed of the nature of the study, agrees to its provisions and has provided written informed consent as approved by the Institutional Review Board (IRB) of the respective clinical site; The subject and the treating physician agree that the subject will return for all required post-procedure follow-up visits; Subject's aortic annulus is 19-27mm diameter as measured by computerized tomography (CT) conducted within 12 months prior to informed consent. Note: if CT is contraindicated and/or not possible to be obtained for certain subjects, a 3D echo and non-contrast CT of chest and abdomen/pelvis may be accepted if approved by the subject selection committee; For a subject to be considered an Extreme Risk candidate they must meet # 2, 3, 4, 5, 6, 7 of the above criteria, and; The subject, after formal consults by a cardiologist and two cardiovascular surgeons agree that medical factors preclude operation, based on a conclusion that the probability of death or serious, irreversible morbidity exceeds the probability of meaningful improvement. Specifically, the probability of death or serious, irreversible morbidity should exceed 50%. The surgeons' consult notes shall specify the medical or anatomic factors leading to that conclusion and include a printout of the calculation of the STS score to additionally identify the risks in these patients.

Exclusion: Evidence of an acute myocardial infarction (defined as: ST Segment Elevation as evidenced on 12 Lead ECG) within 30 days prior to index procedure; Any percutaneous coronary or peripheral interventional procedure performed within 30 days prior to index procedure; Need for emergency surgery for any reason; Active peptic ulcer or upper gastrointestinal (GI) bleeding within 3 months prior to index procedure; Recent (within 6 months prior to index procedure date) cerebrovascular accident (CVA) or a transient ischemic attack (TIA); Currently participating in an investigational drug or device study; Active bacterial endocarditis within 6 months prior to the index procedure; Mixed aortic valve disease (aortic stenosis and aortic regurgitation with predominant aortic regurgitation 3-4+); History of bleeding diathesis or coagulopathy; Cardiogenic shock manifested by low cardiac output, vasopressor dependence, or mechanical hemodynamic support; Untreated clinically significant coronary artery disease requiring revascularization; Hemodynamic instability requiring inotropic support or mechanical heart assistance; A known hypersensitivity or contraindication to aspirin, heparin, ticlopidine (Ticlid), or clopidogrel (Plavix), or sensitivity to contrast media which cannot be adequately premedicated; Life expectancy < 12 months from the time of informed consent due to non-cardiac co-morbid conditions; Significant aortic disease, including abdominal aortic or thoracic aneurysm defined as maximal luminal diameter 5cm or greater; marked tortuosity (hyperacute bend), aortic arch atheroma (especially if thick [> 5 mm], protruding or ulcerated) or narrowing (especially with calcification and surface irregularities) of the abdominal or thoracic aorta, severe "unfolding" and tortuosity of the thoracic aorta (applicable for transfemoral patients only); Subject has a hostile chest or other condition that complicates transaortic access; Subject has a history of patent LIMA/RIMA graft that would preclude access; Additional exclusion criteria for subclavian/axillary access using the FlexNav™ Delivery System:; Pre-existing prosthetic heart valve or other implant in any valve position, prosthetic ring, severe circumferential mitral annular calcification (MAC) which is continuous with calcium in the left ventricular outflow tract (LVOT), severe (greater than 3+) mitral insufficiency, or severe mitral stenosis with pulmonary compromise. Subjects with pre-existing surgical bioprosthetic aortic heart valve should be considered for the Valve-in-Valve registry; Blood dyscrasias as defined: leukopenia (WBC<3000 mm3), acute anemia (Hb < 9 g/dL), thrombocytopenia (platelet count <50,000 cells/mm³); Severe ventricular dysfunction with left ventricular ejection fraction (LVEF) <20% as measured by resting echocardiogram; Renal insufficiency (creatinine > 3.0 mg/dL) and/or end stage renal disease requiring chronic dialysis; Aortic valve is a congenital unicuspid or congenital bicuspid valve or is non-calcified as verified by echocardiography; Hypertrophic cardiomyopathy with or without obstruction (HOCM); Echocardiographic evidence of intracardiac mass, thrombus or vegetation; Native aortic annulus size < 19 mm or > 27 mm per the baseline diagnostic imaging; Aortic root angulation > 70° (applicable for transfemoral patients only); Bulky calcified aortic valve leaflets in close proximity to coronary ostia; Non-calcified aortic annulus; Iliofemoral vessel characteristics that would preclude safe placement of the introducer sheath such as severe obstructive calcification, or severe tortuosity (applicable for transfemoral patients only); Additional Exclusion Criteria (Transcatheter Access Related); For selection of an appropriate alternative access delivery method, subjects were screened using the following access specific exclusion criteria:; Transaortic (TAo) Subject Cohort Specific Exclusion Criteria; Subject has pre-existing patent RIMA graft that would preclude access; Subject has a porcelain aorta, defined as an extensive circumferential calcification of the ascending aorta that would complicate TAo access; Additional exclusion criteria for transaortic access using the FlexNav™ Delivery System:; Subject has a distance between the annular plane and the aortic access site <7 cm (2.8"); Subject has a distance between the annular plane and the separate introducer sheath distal tip <6 cm (2.4"); Subclavian/Axillary Subject Cohort Specific Exclusion Criteria; Subject's access vessel (subclavian/axillary) diameter will not allow for introduction of the applicable 18 Fr or 19 Fr delivery system; Subject's subclavian/axillary arteries have severe calcification and/or tortuosity; Subject's aortic root angulation is:; Left Subclavian/Left Axillary: >70◦; Right Subclavian/Right Axillary: >30◦; Subject's access vessel (subclavian/axillary) has a distance between the annular plane and the integrated sheath distal tip <17 cm (6.7"); Subject's access vessel requires the delivery system to be advanced through a separate introducer sheath.

ClinicalTrials.gov NCT02000115