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Congenital Heart Defects clinical trials

View clinical trials related to Congenital Heart Defects.

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NCT ID: NCT00226369 Completed - Clinical trials for Congenital Heart Defects

Cylexin for Reduction of Reperfusion Injury in Infant Heart Surgery

Start date: December 1997
Phase: Phase 2/Phase 3
Study type: Interventional

We conducted a multicenter, randomized, placebo-controlled trial of Cylexin, an inhibitor of the attachment of white blood cells to the endothelium. Our study population was neonates and infants undergoing hypothermic cardiopulmonary bypass during surgical repair or palliation of congenital heart defects.

NCT ID: NCT00215072 Terminated - Clinical trials for Congenital Heart Defects

Death Following Congenital Heart Surgery

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

The purpose of this study is to elucidate the patterns of death following congenital heart surgery.

NCT ID: NCT00208754 Terminated - Clinical trials for Congenital Heart Defects

Heart Failure in Adult Patients With a History of Congenital Heart Disease

Start date: May 2004
Phase: N/A
Study type: Observational

In today's world of advanced surgery, children born with congenital heart disease (CHD) are surviving into adulthood. However, the surgical procedures these children undergo do not cure the underlying problem and this these children develop other heart problems later in life. Heart failure is the one of the most common heart problems effecting these patients. This heart failure can be seen in both lower pumping chambers of the heart, however, sometimes only one side of the heart is affected. Since there are several congenital heart defects that are now seen in the adult population, an understanding of what causes heart failure in this patient population can help physicians develop better treatments for this condition. The goal of this study is to review the medical records of 350 adult patients with congenital heart disease that has developed heart failure. During this review, we plan to collect information regarding the various treatments utilized in these patients and to determine if there are any common elements regarding the development of heart failure in adult patients with CHD.

NCT ID: NCT00208676 Terminated - Clinical trials for Congenital Heart Defects

Using Tissue Doppler/Synchronization to Determine Heart Function in Children With Congenital Heart Disease

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

There are many children that have heart dysfunction because they are either born with Congenital Heart Disease (CHD) or developed poor heart function because their hearts are ill. The invention of medical technology helps in the treatment of these children. New heart echocardiogram (echo) techniques including Tissue Doppler (TDI), Tissue Synchronization Imaging (TSI) and 3 dimensional echocardiography (3D) are imaging technologies that we hope will help in the diagnosis and treatment of these children. Tissue Doppler Imaging is a noninvasive technique that measures the speed of heart muscle movement. Tissue Synchronization Imaging measures how well the lower pumping chambers of the heart are working together. A 3D echo is a 3 dimensional picture of a beating heart that allows your doctor to see the heart from any angle. These techniques are noninvasive, meaning on the outside of your body. The size and function of the ventricles (the lower part of the heart) can change under different conditions. Using these techniques we will attempt to better determine how well the ventricles function during illness and health.

NCT ID: NCT00115375 Completed - Clinical trials for Congenital Heart Defects

Platelet Aggregation Inhibition in Children on Clopidogrel (PICOLO)

Start date: January 2004
Phase: Phase 2
Study type: Interventional

PICOLO is a double blind placebo controlled phase II dose ranging, dose escalating study in patients of Blalock-Taussig age categories (neonates and infants/toddlers), to determine the dose providing inhibition of platelet aggregation similar to adults.

NCT ID: NCT00112424 Completed - Clinical trials for Congenital Heart Defects

Trial of Cardiac Magnetic Resonance Imaging (MRI) Versus Cardiac Catheterization Prior to Glenn Operation

Start date: January 2004
Phase: N/A
Study type: Interventional

This study is a prospective, randomized study of patients with single ventricle heart disease who are to undergo superior cavo-pulmonary anastomosis, or "Glenn" operation. Such patients have historically undergone cardiac catheterization to ensure suitability for the procedure. Cardiac magnetic resonance imaging (cardiac MRI) is a newer technology that provides excellent anatomic and functional imaging of the heart. This study is designed to demonstrate our hypothesis that cardiac magnetic resonance imaging will provide comparable information to catheterization, with less side effects.

NCT ID: NCT00006186 Completed - Clinical trials for Congenital Heart Defects

Autologous Fresh Whole Blood and Coagulation Following Cardiopulmonary Bypass in Infants

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

Dilution of blood caused by cardiopulmonary bypass (the heart-lung machine) during open heart surgery is associated with decreased concentrations in the blood of coagulation factors. This can be extreme in infants because of their small blood volumes and can lead to impairment of the normal blood clotting mechanism and excessive bleeding after the operation. Transfusion of fresh whole blood has been shown to be an effective treatment because fresh blood is rich in coagulation factors. However, it is difficult to obtain truly fresh blood from a blood bank. We hypothesized that fresh blood drawn from the patient and given back after cardiopulmonary bypass would improve the clotting mechanism. In our study, the infants in the treatment group have some of their own fresh blood removed after they are anesthetized for the operation and before they are placed on cardiopulmonary bypass. This blood is then given back to them after completion of cardiopulmonary bypass. Infants in the control group will not have their own blood removed but will undergo cardiopulmonary bypass. We will compare the two groups by drawing blood samples that measure coagulation tests.