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Heart Defects, Congenital clinical trials

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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: NCT00027417 Completed - Clinical trials for Heart Defects, Congenital

Study of Triostat in Infants During Heart Surgery

Start date: April 2001
Phase: Phase 3
Study type: Interventional

This is a study to determine the safety and efficacy of liothyronine sodium/triiodothyronine (Triostat), a synthetic thyroid hormone, when given to infants with congenital heart disease during cardiopulmonary bypass surgery.

NCT ID: NCT00027196 Completed - Clinical trials for Congenital Heart Defect

Signs and Symptoms Associated With Molecular Defects in Genetically Inherited Heart Disease

Start date: April 1998
Phase: N/A
Study type: Observational

Genetically inherited heart diseases (familial cardiopathies) are conditions affecting the heart passed on to family members by abnormalities in genetic information. These conditions are responsible for many heart related deaths and illnesses. Researchers are interested in learning more about the specific genetic abnormalities causing heart diseases. In addition, they would like to find out how these abnormal genes can contribute to the development of other medical problems. In order to do this, researchers plan to study patients and family members of patients diagnosed with genetically inherited heart disease. Those people participating in the study will undergo a variety of tests including blood tests, echocardiograms, and magnetic resonance imaging studies (MRI). These tests will be used to help researchers find the genetic problem causing the familial cardiopathy. Researchers hope that the information gathered from this study can be used to develop better medical care through early diagnosis, management, and treatment plans.

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.

NCT ID: NCT00006183 Completed - Clinical trials for Cardiovascular Diseases

Comparison of Hematocrit Levels in Infant Heart Surgery

Start date: July 2000
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the effects of diluted hematocrit (HCT) levels of 35% versus 25% during hypothermic cardiopulmonary bypass (CPB) in infants with d-transposition of the great arteries, a malformation of the heart vessels.

NCT ID: NCT00005546 Completed - Clinical trials for Cardiovascular Diseases

Molecular Genetic Epidemiology of Three Cardiac Defects -SCOR in Pediatric Cardiovascular Disease

Start date: January 1999
Phase: N/A
Study type: Observational

To identify genes involved in the pathogenesis of three types of congenital heart disease, atrial septal defects, paramembranous ventricular septal defects, and atrioventricular canal defects.

NCT ID: NCT00005323 Completed - Clinical trials for Cardiovascular Diseases

Epidemiology of Persistent Pulmonary Hypertension of the Newborn - SCOR in Lung Biology and Diseases in Infants and Children

Start date: December 1991
Phase: N/A
Study type: Observational

To conduct an epidemiologic study of persistent pulmonary hypertension of the newborn ( PPHN) infant.

NCT ID: NCT00005322 Completed - Clinical trials for Cardiovascular Diseases

Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease

Start date: January 1990
Phase: N/A
Study type: Observational

To identify genes involved in the pathogenesis of congenital heart disease, including atrial septal defects (ASDs), paramembranous ventricular septal defects (VSDs), and atrioventricular canal defects (AVCDs).

NCT ID: NCT00005258 Completed - Clinical trials for Cardiovascular Diseases

Family Study of Congenital Cardiovascular Malformations

Start date: June 1990
Phase: N/A
Study type: Observational

To determine genetic mechanisms responsible for congenital cardiovascular malformations.

NCT ID: NCT00005190 Completed - Clinical trials for Cardiovascular Diseases

Reproduction and Survival After Cardiac Defect Repair

Start date: July 1986
Phase: N/A
Study type: Observational

To create a registry of all Oregon children undergoing surgical repair of congenital heart disease since 1958 in order to determine mortality, morbidity, and disability after surgery and to assess the safety of pregnancy in women with corrected congenital heart disease and the risk of prematurity and occurrence of congenital heart defects in offspring.