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Aortic Stenosis clinical trials

View clinical trials related to Aortic Stenosis.

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NCT ID: NCT01161732 Completed - Aortic Stenosis Clinical Trials

Early Surgery Versus Conventional Treatment in Very Severe Aortic Stenosis

RECOVERY
Start date: July 2010
Phase: N/A
Study type: Interventional

The optimal timing of surgical intervention remains controversial in asymptomatic patients with very severe aortic stenosis. The investigators therefore try to compare long-term clinical outcomes of early surgery with those of conventional treatment strategy in a prospective randomized trial.

NCT ID: NCT01144039 Completed - Myocardial Ischemia Clinical Trials

Glutamate and Diastolic Function in Patients Undergoing Aortic Valve Repair

Start date: February 2006
Phase: Phase 4
Study type: Interventional

Purpose: The effect of intravenous glutamate infusion on myocardial diastolic function and overall hemodynamics were studied in patients undergoing elective aortic valve replacement with severe aortic stenosis and associated left ventricular hypertrophy . Methods: 25 patients will be included in this double-blind randomized placebo-controlled study. Glutamate was administered intravenously immediately after aortic cross-clamp release. The patients receive either a low dose of 30mg kg-1 h-1 (LG-group) or high dose of 60 mg kg-1 h-1 (HG-group) or placebo (P-group) at a rate of 3.3ml kg-1h-1 for 2h. Transesophageal echocardiography (TEE) is used to measure diastolic and systolic ventricular function before sternotomy (T0), and 2h (T2), 3h (T3) and 6h (T4) after release of cross clamp. Additionally routine hemodynamic parameters are measured intraoperatively.

NCT ID: NCT01115907 Completed - Aortic Stenosis Clinical Trials

Freedom SOLO Stentless Heart Valve Study

SOLO
Start date: December 2010
Phase: Phase 3
Study type: Interventional

The purpose of this clinical investigation is to demonstrate the safety and effectiveness of the Freedom SOLO heart valve.

NCT ID: NCT01060020 Completed - Aortic Stenosis Clinical Trials

Acute Hemodynamic Effects of Sildenafil in Patients With Severe Aortic Stenosis

Start date: January 2010
Phase: Phase 4
Study type: Interventional

Pulmonary hypertension is common in patients with aortic stenosis and is associated with worse operative and long-term outcomes. Sildenafil has been shown to reduce pulmonary artery pressure and improve exercise performance in patients with left-sided heart failure, but this has not been tested in patients with aortic stenosis. We hypothesize that Sildenafil will produce a clinically significant decrease in pulmonary artery pressure in patients with severe aortic stenosis. The dose of Sildenafil that produces a significant decrease in pulmonary artery pressure will be safe and well tolerated in patients with and without a depressed ejection fraction.

NCT ID: NCT01000233 Recruiting - Aortic Stenosis Clinical Trials

Value of Oral Phytate (InsP6) in the Prevention of Progression of the Cardiovascular Calcifications

CALCIFICA
Start date: August 2009
Phase: Phase 2/Phase 3
Study type: Interventional

Intervention study focused on preventing the progression of aortic valve calcification. Vascular and cardiac calcifications are a marker of risk and poor outcome, especially the severe calcified aortic stenosis and coronary calcification. Its increasing prevalence is now a health problem. The knowledge and the therapeutic objective of this condition have changed in recent years and pathophysiological aspects at present, focus on atherosclerotic disease and inflammation. Several clinical trials have failed to demonstrate that statins or ACE inhibitors prevent the progression of cardiovascular calcification. Taking into account the new concepts of ectopic calcification and research results from our group, the most logical approach to prevent progression would be an early intervention and management of the calcification inhibiting agents such as phytate (inositol six-phosphate -- InsP6). Hypothesis: The phytate prevents or delays the progression of cardiovascular calcification. It is a clinical trial of intervention of oral phytate (InsP6) in patients with mild to moderate cardiovascular calcification (aortic valve and / or coronary arteries) compared with placebo over a period of 24 months. It is a prospective, randomized minimization of variables to ensure homogeneity of the groups. The primary analysis will be the time evolution of the extent of calcium in the aortic valve and coronary arteries made with CT. Secondary variables are the degree of progression of aortic stenosis and clinical events (death, stroke, angina, stroke and cancer of any type).

NCT ID: NCT00830726 Recruiting - Heart Failure Clinical Trials

Water- and Salt-homeostasis in Healthy Humans, and in Patients With Heart- or Lung Disease

Start date: February 2009
Phase: N/A
Study type: Observational

The purpose of the study is to determine whether the excretion of renal water- and salt-channels in the urine reflects the handling of water and salt in the kidneys, and whether the excretion can be used to monitor and/or predict the effects of treatment of certain heart or lung diseases.

NCT ID: NCT00805051 Completed - Bleeding Clinical Trials

Acquired Von Willebrand Syndrome in Severe Aortic Stenosis

Start date: October 2008
Phase: N/A
Study type: Observational

Patients with severe aortic stenosis often suffer from an acquired Von Willebrand syndrome by degeneration of the polymers during passage through the narrow valve leading to turbulences. We hypothesized that the diagnosis of acquired von Willebrand syndrome influence perioperative blood loss in patients undergoing open cardiac valve replacement.

NCT ID: NCT00800800 Completed - Aortic Stenosis Clinical Trials

Effects of Rosuvastatin on Aortic Stenosis Progression

ASTRONOMER
Start date: November 2002
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the effects of rosuvastatin compared to usual care in patients diagnosed with aortic valvular stenosis. Patients must have a diagnosis of mild to moderate aortic stenosis (AS) and no clinical indication for the use of cholesterol lowering agents. A multi-centre, randomized, double-blind, placebo-controlled study, with a two year recruitment period, and a treatment duration of a minimum of 3 years from the time of the last patient randomized to a maximum of 5 years.

NCT ID: NCT00788242 Completed - Heart Failure Clinical Trials

The Effect of Glucose-Insulin-Potassium Infusion in Patients Undergoing Cardiac Surgery

Start date: January 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the cardioprotective effects of a short term infusion of glucose-insulin-potassium (GIK) during heart surgery.

NCT ID: NCT00774657 Withdrawn - Aortic Stenosis Clinical Trials

Ventricular Remodeling In Patients With Aortic Stenosis Assessed Echocardiography

Start date: September 2008
Phase: N/A
Study type: Observational

This preliminary study will compare the effectiveness of two-dimensional and three-dimensional echocardiographic measurements of wall thickness and left ventricular mass in patients with Aortic Stenosis