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Heart Valve Diseases clinical trials

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NCT ID: NCT01116037 Terminated - Clinical trials for Heart Valve Diseases

ATS 3f(r) Aortic Bioprosthesis Model 1000 Post Approval Study

PAS
Start date: September 2009
Phase: N/A
Study type: Interventional

The purpose of this clinical study is to determine if there is an increased incidence and rate of aortic regurgitation in younger (</= 70 years of age) patients implanted with the Model 1000 and undergoing isolated aortic valve replacement of his/her native aortic valve, or replacement of a failed prosthesis.

NCT ID: NCT01116024 Completed - Clinical trials for Heart Valve Diseases

ATS 3f Enable(tm) Aortic Bioprosthesis, Model 6000

Enable
Start date: May 2006
Phase: N/A
Study type: Interventional

This is a prospective, non-randomized, multi-center study designed to evaluate safety and effectiveness of the ATS 3f Enable Aortic Bioprosthesis in a patient population undergoing isolated aortic valve replacement with or without concomitant procedures. The Enable Aortic Valve is an equine pericardial stented bioprosthesis.

NCT ID: NCT01076296 Completed - Clinical trials for Pulmonary Hypertension

A Post-Marketing Study for On Label Evaluation of the GE Vscan Ultrasound Imaging System

Start date: February 2010
Phase: N/A
Study type: Observational

This study is to collect data and learn more about the Vscan Ultrasound Imaging System. It is an "observational" study with no additional procedures or intervention prescribed other than using the Vscan along with a routine medical physical exam.

NCT ID: NCT01052948 Completed - Parkinson's Disease Clinical Trials

The Association Between Dopamine Agonists and Cardiac Valvulopathy, Fibrosis and Other Cardiopulmonary Events

Start date: January 2007
Phase: N/A
Study type: Observational

To assess the association between cabergoline and other dopamine agonists (DAs), and symptomatic, diagnosed serious cardiopulmonary disorders, including: 1. Cardiac valve regurgitation 2. Diffuse Pleural/pulmonary thickening and pericardial and retroperitoneal fibrosis 3. Heart failure 4. Total, cardiac and respiratory mortality

NCT ID: NCT01026571 Active, not recruiting - Clinical trials for Bicuspid Aortic Valve

Identification of Genetic Causes of Bicuspid Aortic Valve Disease

BAV Genetics
Start date: December 2009
Phase:
Study type: Observational

BAVgenetics is a partnership between Investigators at Boston University, Brigham and Women's Hospital, and Massachusetts General Hospital dedicated to discovering the genetic causes of bicuspid aortic valve disease and associated aortic disease.

NCT ID: NCT01023152 Completed - Heart Valve Disease Clinical Trials

Effect of Remote Ischemic Preconditioning on Acute Kidney Injury in Patients Undergoing Heart Valve Replacement Surgery With Cardiopulmonary Bypass

Start date: n/a
Phase: N/A
Study type: Interventional

The purpose of this study is to study the effect of remote ischemic preconditioning on acute kidney injury in patients undergoing heart valve replacement surgery with cardiopulmonary bypass.

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: NCT00978588 Completed - Clinical trials for Mitral Valvular Heart Disease

Comparison of 6% Hydroxyethyl Starch 130/0.4 With 5% Albumin as Priming Solution for Cardiopulmonary Bypass

Start date: February 2008
Phase: N/A
Study type: Interventional

Comparison of 6% hydroxyethyl starch 130/0.4 with 5% albumin as priming solution for cardiopulmonary bypass

NCT ID: NCT00934596 Completed - Clinical trials for Aortic Valve Disorder

CO2 Versus Lund De-airing Technique in Heart Surgery

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

To evaluate which of the two de-airing methods (CO2 insufflation vs. Lund de-airing technique) can shorten the left heart de-airing time and prevent or minimize cerebral air emboli during open surgery involving exposure of the left heart to the ambient air. To evaluate the cost effectiveness and possible side effects of CO2 de-airing technique compared to Lund de-airing technique.

NCT ID: NCT00921596 Recruiting - Clinical trials for Heart Valve Diseases

Cardiac Operation Under Totally Endoscope and Cardiopulmonary Bypass (CPB)

CPB
Start date: January 2000
Phase: Phase 1/Phase 2
Study type: Interventional

Conventional cardiac operations are performed with median sternotomy, which is related to great wound, morbidities, longer duration in hospital and most significantly, cosmetic problems. The investigators invested a new minimally invasive cardiac operation method totally under video-endoscope and peripheral cardiopulmonary bypass. The investigators' hypothesis is that this new minimally method could provide better cosmetic effects to the patients, and also relate to shorter postoperative hospital stay and better recovery.