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

Aortic Valve Stenosis Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01437098
• Other study ID #: MDT-2111
• Status: Completed
• Phase: N/A
• Start date: October 2011
• Est. completion date: November 27, 2018

Study information

• Verified date: October 2018
• Source: Medtronic Cardiovascular
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The primary objective of the present trial is to demonstrate the effectiveness and safety of the MDT-2111 in the treatment of symptomatic severe aortic stenosis in subjects deemed difficult for surgical operation.

Description:

Non-randomized, prospective, multicenter, single-arm trial.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 55
• Est. completion date: November 27, 2018
• Est. primary completion date: April 2013
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

1. 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.

2. 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.

3. 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.

4. Subject has been informed of the nature of the trial and has signed an Informed Consent Form.

5. Subject agrees to comply with specified follow-up evaluations and to return to the same investigational site where the procedure was performed.

Exclusion Criteria:

1. Evidence of an acute myocardial infarction = 30 days prior to the intended treatment.

2. Any percutaneous coronary or peripheral interventional procedure performed within 30 days prior to the procedure.

3. Blood dyscrasias as defined:

• Leukopenia (WBC count < 1,000 cells/mm³)

• Thrombocytopenia (platelet count <50,000 cells/mm³)

• History of bleeding diathesis or coagulopathy

• Hypercoagulable states

4. Untreated clinically significant coronary artery disease requiring revascularization.

5. Cardiogenic shock manifested by low cardiac output, vasopressor dependence, or mechanical hemodynamic support.

6. Need for emergency surgery for any reason.

7. Severe ventricular dysfunction with left ventricular ejection fraction (LVEF) < 20% as measured by resting echocardiogram.

8. Recent (within 6 months) cerebrovascular accident (CVA) or transient ischemic attack(TIA).

9. End stage renal disease requiring chronic dialysis.

10. GI bleeding within the past 3 months.

11. A known hypersensitivity or contraindication to any of the following which cannot be adequately pre-medicated:

• Aspirin

• Ticlopidine

• Heparin

• Contrast media

• Nitinol (titanium and nickel alloy)

12. Ongoing sepsis, including active endocarditis.

13. Subject refuses a blood transfusion.

14. Life expectancy < 12 months due to associated non-cardiac co-morbid conditions.

15. Other medical, social, or psychological conditions that in the opinion of an Investigator precludes the subject from appropriate consent.

16. Severe dementia (resulting in either inability to provide informed consent for the trial/procedure, prevents independent lifestyle outside of a chronic care facility, or will fundamentally complicate rehabilitation from the procedure or compliance with follow-up visits).

17. Currently participating in an investigational drug or another device trial. Note:

Trials requiring extended follow-up for products that were investigational, but have since become commercially available, are not considered investigational trials.

18. Symptomatic carotid or vertebral artery disease.

19. Native aortic annulus size < 20 mm or > 27 mm per the screening diagnostic imaging.

20. Pre-existing prosthetic heart valve in any position.

21. Mixed aortic valve disease (aortic stenosis and aortic regurgitation with predominant aortic regurgitation).

22. Mitral regurgitation (moderate to severe) or severe tricuspid regurgitation.

23. Moderate to severe mitral stenosis.

24. Hypertrophic obstructive cardiomyopathy.

25. Echocardiographic evidence of intracardiac mass, thrombus or vegetation.

26. Severe basal septal hypertrophy with an outflow gradient.

27. 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.

28. Congenital bicuspid or unicuspid valve verified by echocardiography.

29. 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.

30. 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.

31. 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.

32. 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

Related Conditions & MeSH terms

• Aortic Valve Stenosis
• Constriction, Pathologic

Intervention

Device:
• MDT-2111 CoreValve for TAVI
CoreValve Transcatheter Aortic Valve Implantation (TAVI) using the MDT-2111 system.

Locations

Country	Name	City	State
Japan	Saitama Medical University	Hidaka	Saitama
Japan	Shonan Kamakura General Hospital	Kamakura	Kanagawa
Japan	National Cerebral and Cardiovascular Center	Suita	Osaka
Japan	Osaka University Hospital	Suita	Osaka

Sponsors (1)

Lead Sponsor	Collaborator
Medtronic Cardiovascular

Country where clinical trial is conducted

Japan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Composite Success of Improvement in New York Heart Association (NYHA) Class and a Performance Goal for Effective Orifice Area (EOA).	The primary endpoint was defined as the proportion of implanted subjects with improvement of at least 1 NYHA class from baseline to 6 months and EOA greater than 1.2 cm² at 6 months.	baseline and 6 months
Secondary	NYHA Classification Over Time	NEW YORK HEART ASSOCIATION CLASSIFICATION (NYHA) Class I Subject with cardiac disease but without resulting limitations of physical activity. Ordinary physical activity does not cause undue fatigue, palpitation, dyspnea, or anginal pain.; Class II Subjects with cardiac disease resulting in slight limitation of physical activity. They are comfortable at rest. Ordinary physical activity results in fatigue, palpitation, dyspnea, or anginal pain.; Class III Subjects with cardiac disease resulting in marked limitation of physical activity. They are comfortable at rest. Less than ordinary physical activity causes fatigue, palpitation, dyspnea, or anginal pain. Class IV Subjects with cardiac disease resulting in inability to carry on any physical activity without discomfort. Symptoms of cardiac insufficiency or of the anginal syndrome may be present even at rest. If any physical activity is undertaken, discomfort is increased.	30 days
Secondary	NYHA Classification Over Time	NEW YORK HEART ASSOCIATION CLASSIFICATION (NYHA) Class I Subject with cardiac disease but without resulting limitations of physical activity. Ordinary physical activity does not cause undue fatigue, palpitation, dyspnea, or anginal pain.; Class II Subjects with cardiac disease resulting in slight limitation of physical activity. They are comfortable at rest. Ordinary physical activity results in fatigue, palpitation, dyspnea, or anginal pain.; Class III Subjects with cardiac disease resulting in marked limitation of physical activity. They are comfortable at rest. Less than ordinary physical activity causes fatigue, palpitation, dyspnea, or anginal pain. Class IV Subjects with cardiac disease resulting in inability to carry on any physical activity without discomfort. Symptoms of cardiac insufficiency or of the anginal syndrome may be present even at rest. If any physical activity is undertaken, discomfort is increased.	6 months
Secondary	NYHA Classification Over Time	NEW YORK HEART ASSOCIATION CLASSIFICATION (NYHA) Class I Subject with cardiac disease but without resulting limitations of physical activity. Ordinary physical activity does not cause undue fatigue, palpitation, dyspnea, or anginal pain.; Class II Subjects with cardiac disease resulting in slight limitation of physical activity. They are comfortable at rest. Ordinary physical activity results in fatigue, palpitation, dyspnea, or anginal pain.; Class III Subjects with cardiac disease resulting in marked limitation of physical activity. They are comfortable at rest. Less than ordinary physical activity causes fatigue, palpitation, dyspnea, or anginal pain.; Class IV Subjects with cardiac disease resulting in inability to carry on any physical activity without discomfort. Symptoms of cardiac insufficiency or of the anginal syndrome may be present even at rest. If any physical activity is undertaken, discomfort is increased.	12 Months
Secondary	NYHA Classification Over Time	NEW YORK HEART ASSOCIATION CLASSIFICATION (NYHA) Class I Subject with cardiac disease but without resulting limitations of physical activity. Ordinary physical activity does not cause undue fatigue, palpitation, dyspnea, or anginal pain.; Class II Subjects with cardiac disease resulting in slight limitation of physical activity. They are comfortable at rest. Ordinary physical activity results in fatigue, palpitation, dyspnea, or anginal pain.; Class III Subjects with cardiac disease resulting in marked limitation of physical activity. They are comfortable at rest. Less than ordinary physical activity causes fatigue, palpitation, dyspnea, or anginal pain.; Class IV Subjects with cardiac disease resulting in inability to carry on any physical activity without discomfort. Symptoms of cardiac insufficiency or of the anginal syndrome may be present even at rest. If any physical activity is undertaken, discomfort is increased.	24 Months
Secondary	NYHA Classification Over Time	NEW YORK HEART ASSOCIATION CLASSIFICATION (NYHA) Class I Subject with cardiac disease but without resulting limitations of physical activity. Ordinary physical activity does not cause undue fatigue, palpitation, dyspnea, or anginal pain.; Class II Subjects with cardiac disease resulting in slight limitation of physical activity. They are comfortable at rest. Ordinary physical activity results in fatigue, palpitation, dyspnea, or anginal pain.; Class III Subjects with cardiac disease resulting in marked limitation of physical activity. They are comfortable at rest. Less than ordinary physical activity causes fatigue, palpitation, dyspnea, or anginal pain.; Class IV Subjects with cardiac disease resulting in inability to carry on any physical activity without discomfort. Symptoms of cardiac insufficiency or of the anginal syndrome may be present even at rest. If any physical activity is undertaken, discomfort is increased.	36 Months
Secondary	Major Adverse Cardiovascular and Cerebrovascular Event (MACCE)	MACCE is defined as a composite of: all-cause death; myocardial infarction (MI); all stroke, and; reintervention (defined as any cardiac surgery or percutaneous reintervention catheter procedure that repairs, otherwise alters or adjusts, or replaces a previously implanted valve)	0 day to 30 days
Secondary	Major Adverse Cardiovascular and Cerebrovascular Event (MACCE)	MACCE is defined as a composite of: all-cause death; myocardial infarction (MI); all stroke, and; reintervention (defined as any cardiac surgery or percutaneous reintervention catheter procedure that repairs, otherwise alters or adjusts, or replaces a previously implanted valve)	0 day to 6 months
Secondary	Major Adverse Cardiovascular and Cerebrovascular Event (MACCE)	MACCE is defined as a composite of: all-cause death; myocardial infarction (MI); all stroke, and; reintervention (defined as any cardiac surgery or percutaneous reintervention catheter procedure that repairs, otherwise alters or adjusts, or replaces a previously implanted valve)	0 day to 12 months
Secondary	Major Adverse Cardiovascular and Cerebrovascular Event (MACCE)	MACCE is defined as a composite of: all-cause death; myocardial infarction (MI); all stroke, and; reintervention (defined as any cardiac surgery or percutaneous reintervention catheter procedure that repairs, otherwise alters or adjusts, or replaces a previously implanted valve)	0 day to 24 months
Secondary	Major Adverse Cardiovascular and Cerebrovascular Event (MACCE)	MACCE is defined as a composite of: all-cause death; myocardial infarction (MI); all stroke, and; reintervention (defined as any cardiac surgery or percutaneous reintervention catheter procedure that repairs, otherwise alters or adjusts, or replaces a previously implanted valve)	0 day to 36 months
Secondary	Device Success as Defined in the Description.	successful vascular access, delivery and deployment of the device, and successful retrieval of the delivery system; correct position of the device in the proper anatomical location (placement in the annulus with no impedance on device function); Intended performance of the prosthetic valve (aortic valve area >1.2 cm² (by echocardiography using the continuity equation) and mean aortic valve gradient < 20 mmHg or peak velocity < 3 m/sec, without moderate or severe prosthetic valve AR); Only one valve implanted in the proper anatomical location	after procedure or discharge
Secondary	Procedural Success, Defined as Device Success and Absence of In-hospital MACCE.		after procedure or discharge
Secondary	Echocardiographic Assessment of Prosthetic Valve Performance - Mean Gradient		30 days
Secondary	Echocardiographic Assessment of Prosthetic Valve Performance- Mean Gradient		6 months
Secondary	Echocardiographic Assessment of Prosthetic Valve Performance - Mean Gradient		12 months
Secondary	Echocardiographic Assessment of Prosthetic Valve Performance - Mean Gradient		24 months
Secondary	Echocardiographic Assessment of Prosthetic Valve Performance - Mean Gradient		36 months
Secondary	Echocardiographic Assessment of Prosthetic Valve Performance- Effective Orifice Area (EOA)		30 days
Secondary	Echocardiographic Assessment of Prosthetic Valve Performance- Effective Orifice Area (EOA)		6 months
Secondary	Echocardiographic Assessment of Prosthetic Valve Performance- Effective Orifice Area (EOA)		12 months
Secondary	Echocardiographic Assessment of Prosthetic Valve Performance- Effective Orifice Area (EOA)		24 months
Secondary	Echocardiographic Assessment of Prosthetic Valve Performance- Effective Orifice Area (EOA)		36 months
Secondary	Echocardiographic Assessment of Prosthetic Valve Performance - Left Ventricular Ejection Fraction (LVEF)		30 days
Secondary	Echocardiographic Assessment of Prosthetic Valve Performance - Left Ventricular Ejection Fraction (LVEF)		6 months
Secondary	Echocardiographic Assessment of Prosthetic Valve Performance - Left Ventricular Ejection Fraction (LVEF)		12 months
Secondary	Echocardiographic Assessment of Prosthetic Valve Performance - Left Ventricular Ejection Fraction (LVEF)		24 months
Secondary	Echocardiographic Assessment of Prosthetic Valve Performance - Left Ventricular Ejection Fraction (LVEF)		36 months
Secondary	Echocardiographic Assessment of Prosthetic Valve Performance - Total Aortic Valve Regurgitation (Transvalvular & Paravalvular) (Total AR)		30 days
Secondary	Echocardiographic Assessment of Prosthetic Valve Performance - Total Aortic Valve Regurgitation (Transvalvular & Paravalvular) (Total AR)		6 months
Secondary	Echocardiographic Assessment of Prosthetic Valve Performance - Total Aortic Valve Regurgitation (Transvalvular & Paravalvular) (Total AR)		12 months
Secondary	Echocardiographic Assessment of Prosthetic Valve Performance - Total Aortic Valve Regurgitation (Transvalvular & Paravalvular) (Total AR)		24 months
Secondary	Echocardiographic Assessment of Prosthetic Valve Performance - Total Aortic Valve Regurgitation (Transvalvular & Paravalvular) (Total AR)		36 months
Secondary	Repeat Hospitalization		0 day to 30 days
Secondary	Repeat Hospitalization		0 day to 6 months
Secondary	Repeat Hospitalization		0 day to 12 months
Secondary	Repeat Hospitalization		0 day to 24 months
Secondary	Repeat Hospitalization		0 day to 36 months
Secondary	Valve-related Deaths		0 day to 30 days
Secondary	Valve-related Deaths		0 day to 6 months
Secondary	Valve-Related Deaths		0 day to 12 months
Secondary	Valve-related Deaths		0 day to 24 months
Secondary	Valve-related Deaths		0 day to 36 months
Secondary	Quality of Life Assessment Using SF-36 Questionnaire - Physical Component Summary (Paired Change From Baseline) (Q of L)	The SF-36 assessment was used to evaluate subject Quality of life (QoL) by assessing change in physical function and general health status. The SF-36 v2TM Scoring Program2,3 was used to convert raw scores ranging from 0 to 100 into norm-based scores, allowing direct comparison to the reference values for the Japanese population. A norm-based score of less than 50 was interpreted as below average when compared to the Japanese population whereas norm-based scores greater than 50 were interpreted as above average.	Baseline to 30 days
Secondary	Quality of Life Assessment Using SF-36 Questionnaire - Physical Component Summary (Paired Change From Baseline) (Q of L)	The SF-36 assessment was used to evaluate subject Quality of life (QoL) by assessing change in physical function and general health status. The SF-36 v2TM Scoring Program2,3 was used to convert raw scores ranging from 0 to 100 into norm-based scores, allowing direct comparison to the reference values for the Japanese population. A norm-based score of less than 50 was interpreted as below average when compared to the Japanese population whereas norm-based scores greater than 50 were interpreted as above average.	Baseline to 6 months
Secondary	Quality of Life Assessment Using SF-36 Questionnaire - Physical Component Summary (Paired Change From Baseline) (Q of L)	The SF-36 assessment was used to evaluate subject Quality of life (QoL) by assessing change in physical function and general health status. The SF-36 v2TM Scoring Program2,3 was used to convert raw scores ranging from 0 to 100 into norm-based scores, allowing direct comparison to the reference values for the Japanese population. A norm-based score of less than 50 was interpreted as below average when compared to the Japanese population whereas norm-based scores greater than 50 were interpreted as above average.	Baseline to 12 months
Secondary	Quality of Life Assessment Using SF-36 Questionnaire - Physical Component Summary (Paired Change From Baseline) (Q of L)	The SF-36 assessment was used to evaluate subject Quality of life (QoL) by assessing change in physical function and general health status. The SF-36 v2TM Scoring Program2,3 was used to convert raw scores ranging from 0 to 100 into norm-based scores, allowing direct comparison to the reference values for the Japanese population. A norm-based score of less than 50 was interpreted as below average when compared to the Japanese population whereas norm-based scores greater than 50 were interpreted as above average.	Baseline to 24 Months
Secondary	Quality of Life Assessment Using SF-36 Questionnaire - Physical Component Summary (Paired Change From Baseline) (Q of L)	The SF-36 assessment was used to evaluate subject Quality of life (QoL) by assessing change in physical function and general health status. The SF-36 v2TM Scoring Program2,3 was used to convert raw scores ranging from 0 to 100 into norm-based scores, allowing direct comparison to the reference values for the Japanese population. A norm-based score of less than 50 was interpreted as below average when compared to the Japanese population whereas norm-based scores greater than 50 were interpreted as above average.	Baseline to 36 Months