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Aortic Stenosis clinical trials

View clinical trials related to Aortic Stenosis.

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NCT ID: NCT01658345 Completed - Aortic Stenosis Clinical Trials

Microvascular Dysfunction in Aortic Stenosis

PRIMID-AS
Start date: April 2012
Phase: N/A
Study type: Observational

Aortic stenosis (AS), or narrowing of the aortic valve, is the commonest condition requiring valve surgery in the developed world. It is currently not known what determines who will go on to develop symptoms. Exercise testing may be able to identify these patients better than the severity of the narrowing itself, but with some limitations. The purpose of this study is to compare whether MRI scanning or exercise testing can better identify patients with AS who are likely to benefit from surgery. Design: The investigators will measure blood flow to the heart muscle with MRI scanning and perform exercise testing in 170 patients with AS and follow them for up to up to 2 years. Expected outcomes: MRI scanning will more accurately identify those patients with AS who will need surgery during this period. Anticipated Health Benefits: improved selection of patients with AS who are likely to benefit from early surgery. This is likely to reduce deaths in such patients.

NCT ID: NCT01645202 Completed - Aortic Stenosis Clinical Trials

A Comparison of Transcatheter Heart Valves in High Risk Patients With Severe Aortic Stenosis: The CHOICE Trial

CHOICE
Start date: March 2012
Phase: N/A
Study type: Interventional

A randomized controlled multicenter study comparing the acute hemodynamic performance of the Edwards Sapien XT and the Medtronic CoreValve transcatheter heart valves in high risk patients with severe symptomatic aortic stenosis.

NCT ID: NCT01638156 Completed - Aortic Stenosis Clinical Trials

Cardiac MRI for Severe Aortic Stenosis

Start date: June 2013
Phase:
Study type: Observational

This study will evaluate the importance of arterial stiffness and wave reflections as determinants of persistent left ventricular (LV) hypertrophy and fibrosis (assessed using cardiac magnetic resonance imaging [MRI]) after correction of severe stenosis of the aortic valve. The hypothesis will test whether stiff arteries and increased wave reflections impede pumping of blood by the LV after aortic valve replacement (AVR)and precent adequate regression (improvement) of hypertrophy and fibrosis of the myocardium despite correction of aortic valve stenosis.

NCT ID: NCT01605669 Completed - Aortic Stenosis Clinical Trials

Correlation of Auscultatory Severity of Aortic Stenosis With Trans Thoracic Echocardiography

Cassette
Start date: May 2012
Phase: N/A
Study type: Observational

According to the 2006 ACC/AHA practice guidelines for valvular heart disease, patients with asymptomatic aortic stenosis(AS) should have screening transthoracic echocardiograms (TTE) performed annually for severe disease, every 1-2 years for moderate disease and every 3-5 years for mild disease. This results in a multitude of screening studies in the investigators patient population. 3M has developed a new stethoscope and phonocardiography software capable of identifying the peak intensity of the AS murmur and tracking it as it moves towards the second heart sound potentially indicating increasing severity of disease. Currently there exists no data to demonstrate that the aortic stenosis acceleration index (ASAI) correlates to disease severity or progression of disease. The ASAI measures the timing of the peak intensity of the systolic murmur and compares it to the total time in systole (S2-x/s2-s1) where s1 is the first heart sound; S2 is the second heart sound and x with the time between S1 and the peak intensity of the murmur. In this study the investigators propose to correlate the ASAI to standard TTE measurements of aortic stenosis severity.

NCT ID: NCT01598844 Completed - Aortic Stenosis Clinical Trials

JUPITER Study: Transapical Aortic Valve Implantation for Aortic Regurgitation

JUPITER
Start date: May 30, 2012
Phase:
Study type: Observational

The purpose of this registry is to observe longterm performance and safety of the JenaValve TAVI system, in routine medical and everyday conditions.

NCT ID: NCT01539746 Completed - Aortic Stenosis Clinical Trials

Transcatheter Aortic Valve Implantation Without Predilation

SIMPLIFy TAVI
Start date: January 9, 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to demonstrate that the avoidance of balloon valvuloplasty for predilation of the native aortic valve is associated with a reduction of the composite primary endpoint in TAVI patients with severely impaired left-ventricular ejection fraction (LVEF ≤35%).

NCT ID: NCT01448421 Completed - Aortic Stenosis Clinical Trials

DEFLECT I: Keystone Heart Embolic Deflection Trial

Start date: March 2012
Phase: N/A
Study type: Interventional

This is a research study using the Keystone Heart Embolic Deflection Device and involving patients with aortic stenosis (a disease of the aortic valve), to be treated with Transcatheter Aortic Valve Replacement (TAVR). The TAVR procedure consists in replacing the diseased aortic valve by a new artificial valve. The new valve is put into place using a long, thin tube called a catheter that is inserted into a small incision (cut) in the patient's groin and threaded through his/her arteries up to the heart.

NCT ID: NCT01422044 Completed - Aortic Stenosis Clinical Trials

Risk Prediction in Aortic Stenosis

PREDICT-AS
Start date: September 2009
Phase: N/A
Study type: Observational

The purpose of this study is to test the prognostic value of autonomic markers in patients with aortic stenosis.

NCT ID: NCT01404975 Completed - Aortic Stenosis Clinical Trials

TAVI Protocol - Paravertebral Block Study

TAVI PVB
Start date: June 2011
Phase: N/A
Study type: Interventional

Trans-apical aortic valve replacement is a new treatment for severe aortic stenosis. It is offered to elderly patients with medical problems that would markedly increase the risk of conventional cardiac surgery. The rate of delirium (acute confusional state) after surgery in these patients may exceed 50%. Estimated hospital costs associated with delirium at Toronto General Hospital last year exceeded $1-million CAD. Pain after surgery and the use of opioids (morphine type of pain-relief drugs) are known to increase the risk of delirium. The investigators plan to minimize the use of opioids and improve pain management by replacing the standard intravenous opioid-based pain management with the paravertebral nerve block using only the local anesthetic. These two management strategies will be compared with respect to the rate of delirium, duration of hospital stay, and the overall costs. Hypothesis: Paravertebral analgesia with LA decreases the incidence of delirium after trans-apical AVR when compared to standard systemic opioid-based analgesia.

NCT ID: NCT01395303 Completed - Stroke Clinical Trials

Polymorphisms in the Vitamin D System and Health

Start date: April 2011
Phase: N/A
Study type: Observational

Polymorphisms in the vitamin D system appear to affect the serum 25(OH)D levels. If so one would expect these polymorphisms to be associated with vitamin D related conditions and diseases, which will be tested in the present study including DNA analyses in 9700 subjects