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Heart Valve Diseases clinical trials

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NCT ID: NCT01175681 Completed - Clinical trials for Heart Valve Diseases

Effect of Remote Ischemia Preconditioning on Myocardial Injury in Patients Undergoing Heart Valve Surgery

Start date: December 2007
Phase: N/A
Study type: Interventional

Remote ischaemic preconditioning has shown its cardiac protective effect during heart surgery including coronary artery bypass graft surgery, congenital heart disease and aneurysm. However, no data was reported on heart valve disease surgery. Rheumatic heart disease is one of the major heart diseases requiring surgery in China. Thus, the investigators chose heart valve disease as a focus to see whether remote ischaemic preconditioning also has cardiac protective effect during heart valve surgery.

NCT ID: NCT01174719 Completed - Clinical trials for Coronary Artery Disease

Humanalbumin, Hydroxyethylstarch and Ringer Lactate During Cardiac Surgery

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

The aim of the study is to compare three different regimens for volume replacement during cardiac surgery, e.g. Albumin 5%, Hydroxyethylstarch 130/0.4 (HES) and Ringer-Lactate (RL). Main Outcome parameters: chest tube drainage and coagulation parameters. The investigators hypothesis is that HES is as safe as Albumin, however less expensive. Whether RL is an even less expensive and as safe alternative has to be shown.

NCT ID: NCT01144546 Completed - Clinical trials for Ischemic Heart Disease

Passive Leg Raising Test to Predict Hypotension During Induction of Anesthesia in Patients Undergoing Cardiac Surgery

Start date: August 2009
Phase: Phase 2
Study type: Interventional

Hypotension frequently occurs during anesthesia induction. Preload decrease by anesthetics was often considered as one of main causes for this hypotension. However, the studies on this topic have been lacking. Dynamic preload indices are more suitable than static preload indices to predict the effect of preload changes. And, recently, passive leg raising test showed successful results to predict fluid responsiveness in patient with spontaneous ventilation. The investigators hypothesized that hypotension after induction of anesthesia is caused by decrease of preload by anesthetics and passive leg raising test could predict this hypotension. In this study, the investigators will try to evaluate whether passive leg raising induced hemodynamic changes could predict hypotension during anesthesia induction.

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: 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: 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: NCT00883285 Completed - Clinical trials for Aortic Valve Disease

Incidence and Severity of Silent and Apparent Cerebral Embolism After Conventional and Minimal-invasive Transfemoral Aortic Valve Replacement

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

The purpose of this study is to compare the incidence of silent and apparent cerebral embolism between conventional and minimal-invasive transfemoral aortic valve repair.