Clinical Evaluation of MDT-2111 in Subjects With Symptomatic Severe Aortic Stenosis

Inclusion Criteria

• Subject must have co-morbidities such that one cardiologist and one cardiac surgeons agree that medical factors preclude operation, based on a conclusion that the probability of death or serious morbidity exceeds the probability of meaningful improvement.
• Subject has senile degenerative aortic valve stenosis with:

mean gradient > 40 mmHg or jet velocity greater than 4.0 m/s by either resting or dobutamine stress echocardiogram, or simultaneous pressure recordings at cardiac catheterization (either resting or dobutamine stress), AND an initial aortic valve area of ≤ 0.8 cm² (or aortic valve area index ≤ 0.5 cm²/m²) by resting echocardiogram.

• Subject is symptomatic from his/her aortic valve stenosis, as demonstrated by NYHA Functional Class Class III or greater. If screening committee agrees the eligibility of a patient with class II , based on medical factors, he/she can be enrolled.
• Subject has been informed of the nature of the trial and has signed an Informed Consent Form.
• Subject agrees to comply with specified follow-up evaluations and to return to the same investigational site where the procedure was performed.

Exclusion Criteria

• Evidence of an acute myocardial infarction ≤ 30 days prior to the intended treatment.
• Any percutaneous coronary or peripheral interventional procedure performed within 30 days prior to the procedure.
• Blood dyscrasias as defined:
• Leukopenia (WBC count 27 mm per the screening diagnostic imaging.
• Pre-existing prosthetic heart valve in any position.
• Mixed aortic valve disease (aortic stenosis and aortic regurgitation with predominant aortic regurgitation).
• Mitral regurgitation (moderate to severe) or severe tricuspid regurgitation.
• Moderate to severe mitral stenosis.
• Hypertrophic obstructive cardiomyopathy.
• Echocardiographic evidence of intracardiac mass, thrombus or vegetation.
• Severe basal septal hypertrophy with an outflow gradient.
• Ascending aorta diameter > 43 mm (in case of the aortic annulus is 23-27 mm) unless the aortic annulus is 20-23 mm in which case the ascending aorta diameter > 40 mm.
• Congenital bicuspid or unicuspid valve verified by echocardiography.
• For patients with native coronary artery dependent circulation:
• Sinus of valsalva width < 29 mm unless the aortic annulus is 20-23 mm, in which case the sinus of valsalva width < 27 mm, OR
• Height of the left or right coronary sinus of valsalva (to the tubular aorta) < 15mm.
• Femoral or iliac artery of the first choice corresponding to any one of the followings:
• Angle at aortic root (the angle between aortic valve annulus plane and horizontal plane/vertebra) exceeds 70°.
• Vessel diameter of femoral or iliac artery is less than 6 mm.
• Aorta has severe calcification, excess tortuosity or severe atherosclerosis.
• Transarterial access not able to accommodate an 18Fr sheath.
• Subclavian artery of the second choice corresponding to any one of the followings:
• Angle at aortic root (the angle between aortic valve annulus plane and horizontal plane/vertebra) exceeds 70° (in the case of left subclavian artery) and 30° (in the case of right subclavian artery).
• Vessel diameter of subclavian artery is less than 6 mm.
• Transarterial access not able to accommodate an 18Fr sheath.
• Direct Aortic Artery as third line choice of access. Patients are excluded from Direct Aortic access if:
• Access site is less than 6 cm from the aortic valve basal plane
• Access site has calcification or porcelain aorta
• Access site and delivery trajectory contain RIMA or patent RIMA graft