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Aortic Valve Stenosis clinical trials

View clinical trials related to Aortic Valve Stenosis.

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NCT ID: NCT01475799 Active, not recruiting - Clinical trials for Aortic Valve Stenosis

Percutaneous Aortic Valve 18F System for the Treatment of Patients With Severe Aortic Stenosis

Start date: November 2011
Phase: N/A
Study type: Interventional

The purpose of the study is to determine the safety and performance of the Direct Flow Medical study valve and delivery procedure.

NCT ID: NCT01057173 Active, not recruiting - Clinical trials for Critical Aortic Stenosis

The Nordic Aortic Valve Intervention Trial

NOTION
Start date: December 2009
Phase: N/A
Study type: Interventional

A randomized clinical trial of transcatheter aortic valve implantation (TAVI) versus conventional surgical aortic valve replacement (SAVR) in patients older than 70 years of age suffering from severe aortic valve stenosis. Study hypothesis: TAVI will reduce post-interventional morbidity and mortality compared to SAVR.

NCT ID: NCT00722748 Active, not recruiting - Clinical trials for Coronary Artery Disease

Genomic Investigation of Cardiovascular Diseases

Start date: June 2007
Phase:
Study type: Observational

This proposal puts forward a research plan to initiate a genetic databank, henceforth referred to as The Genebank at Scripps Clinic Registry. This database will usher in genomic research at Scripps as we strive to stay at the forefront of cardiovascular research in the new century. Human subject donation allows for the creation of the proposed genebank.

NCT ID: NCT00530894 Active, not recruiting - Clinical trials for Critical Aortic Stenosis

THE PARTNER TRIAL: Placement of AoRTic TraNscathetER Valve Trial

PARTNER
Start date: April 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the safety and effectiveness of the device and delivery systems (transfemoral and transapical) in high risk, symptomatic patients with severe aortic stenosis.

NCT ID: NCT00375336 Active, not recruiting - Aortic Stenosis Clinical Trials

Risk Factors Associated With Calcification of the Aortic Valve

Start date: January 2005
Phase: N/A
Study type: Observational

The purpose of this study is - to determine the degree of endothelial dysfunction and inflammation in calcific aortic valve disease associated with coronary artery disease(CAD). - to determine whether there is relationship between calcium metabolism and calcific aortic valve disease associated with CAD.

NCT ID: NCT00338676 Active, not recruiting - Aortic Stenosis Clinical Trials

Aortic Stenosis in Elderly : Determinant of Progression

Start date: November 2006
Phase: N/A
Study type: Observational

Aortic stenosis (AS) is AS is caused by calcium deposits in the aortic valve. Calcification is progressive and eventually leads to reduced leaflet motion with obstruction of the left ventricular outflow. The only treatment is surgery. There are evidences that AS is a regulated process with similarities to atherosclerosis but determinants of AS progression are unknown. The study aims at evaluating these determinants and more specifically the role of lipids, inflammation and platelet aggregation.

NCT ID: NCT00294775 Active, not recruiting - Atrial Fibrillation Clinical Trials

Effect of Angiotensin II Receptor Blockers (ARB) on Left Ventricular Reverse Remodelling After Aortic Valve Replacement in Severe Valvular Aortic Stenosis

Start date: February 2006
Phase: Phase 3
Study type: Interventional

The consequence of aortic valve stenosis (AVS) is increased pressure load on the left ventricle which causes left ventricular (LV) hypertrophy, and myocardial stretch will cause activation of cardiac peptides and activation of the renin angiotensin aldosterone system (RAAS). The consequence of LV hypertrophy is increased chamber-stiffness and delayed active LV relaxation which initially will cause diastolic and later systolic dysfunction. In heart failure (HF) and ischemic heart disease the degree of diastolic dysfunction has been demonstrated to correlate with functional class, neurohormonal activation and prognosis which also recently have been suggested for AVS. With longstanding elevated filling pressures the left atrium (LA) will dilate. Only limited data are available on the degree and importance of LA dilatation in AVS. When apparent, symptoms of HF in AVS are associated with high mortality rates. If LV systolic dysfunction also is present prognosis will deteriorate further. In these cases aorta valve replacement (AVR) is recommended. AVR will normalize pressure overload and thereby decreases LV hypertrophy. Previously it was believed that in time LV hypertrophy regressed towards normal and even normalized. Recent studies however have demonstrated that LV hypertrophy regression mainly happens during the first year after AVR, and little subsequent changes are seen during the remaining 10 years. Furthermore, patients that experience most regression of hypertrophy have more favourable outcome and better functional class than patients with less regression of hypertrophy. Thus absence of reverse remodelling is associated with poor outcome after AVR. Importantly the regression of LV hypertrophy is closely paralleled by decreasing RAAS hyperactivity. RAAS hyperactivity may be attenuated pharmacologically with angiotensin II receptor blockers (ARB) which in systemic hypertension with LV hypertrophy has been associated with reverse remodelling. The hypothesis is that in patients undergoing AVR for symptomatic AVS, 12 months post operative blockade of the angiotensin II receptor will accelerate LV and LA reverse remodelling, reduce filling pressures and suppress neurohormonal activation compared with conventional therapy. This will lead to improved exercise tolerance and due to improved left atrial function reducing the risk of atrial arrythmias.