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Heart Defects, Congenital clinical trials

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NCT ID: NCT00284570 Completed - Sepsis Clinical Trials

Pro-Calcitonin Levels Following Pediatric Cardiac Surgery

Start date: January 2006
Phase: N/A
Study type: Observational

First, we, the researchers, hope to find out the PCT response to heart surgery in children by taking blood before surgery and each day for four days after surgery. These blood draws will help us figure out the typical Procalcitonin (PCT) response, the normal increase in PCT after heart surgery, and when the PCT level returns to baseline. Second, we, the researchers, hope to determine the accuracy of PCT as a marker of infection. Hypothesis Our hypothesis is that Procalcitonin is superior to other currently used markers of infection and will prove to be a clinically useful tool for evaluation of infection in children following cardiac surgery.

NCT ID: NCT00281671 Terminated - Clinical trials for Cardiopulmonary Bypass

Nesiritide Use Following Cardiac Surgery in Infants

Start date: April 8, 2006
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine the effects of nesiritide on urine output and hemodynamics following cardiopulmonary bypass in infants. Safety and pharmacokinetic data will also be obtained.

NCT ID: NCT00278005 Terminated - Clinical trials for Congenital Heart Defects

Infection in DiGeorge Following CHD Surgery

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

We propose a retrospective review of patients with DiGeorge syndrome having undergone cardiac surgery to evaluate the incidence of blood stream and/or surgical site infection. The hypothesis is that we will find an increased number of infections for this sub-group. We will compare the incidence of infection to children of similar age and diagnosis to evaluate for variances in the incidence of infection.

NCT ID: NCT00276237 Completed - Clinical trials for Heart Disease, Congenital

Outcomes Following Pulmonary Valve Replacement in Adults

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

One of the most common residual lesions in adult survivors of pediatric cardiac surgery is pulmonary valve disease, particularly regurgitation. Multiple studies have demonstrated that placement of a pulmonary valve in such patients, results in improved ventricular function and resolution of symptoms. However, the optimal prosthetic valve for use in the pulmonary position has not been defined. There are essentially three alternatives available: the stented bioprosthetic valve, stentless bioprosthetic "tube" grafts used to replace the entire right ventricular outflow tract and mechanical valves. All three of these valve options have been used in adults with congenital heart disease at Emory Healthcare and at Children's Healthcare of Atlanta at Egleston. The goal of this study is to evaluate and compare the indications and short and mid-term outcomes for these alternative therapies.

NCT ID: NCT00266201 Completed - Heart Failure Clinical Trials

Right Ventricular Failure in Congenital Heart Defects

Start date: June 2003
Phase: N/A
Study type: Observational

Usually, "heart failure" refers to myocardial insufficiency of the left ventricle. However, in patients with congenital heart defects, often predominantly the right ventricle is affected. Brain natriuretic peptide (BNP) has been shown to be a reliable biomarker for left ventricular function and severity of left ventricular failure. The objective of the present investigation is to evaluate brain natriuretic peptide (BNP) with regard to its predictive value as a biomarker for right ventricular function, clinical symptoms and/or the patients' quality of life.To this end, blood levels of neurohumoral markers are measured and tested for statistical correlation with exercise tolerance and right ventricular function, as assessed by imaging methods. A sample of healthy volunteers serves as a control group.

NCT ID: NCT00257777 Completed - Clinical trials for Coronary Artery Disease

Intermittent Cold Blood vs Crystalloid Cardioplegia in Aortic Valve Surgery

Start date: November 2003
Phase: N/A
Study type: Interventional

Controversies still exists concerning the overall clinical effects of blood-based vs. crystalloid- based cardioplegic solution for myocardial protection during cardiac arrest. Both techniques are used world-wide. No larger prospectively randomized studies comparing the two methods have been reported. The aim of this study is to collect a large number of clinical data to create a proper basis for evaluation of the two techniques.

NCT ID: NCT00243776 Recruiting - Clinical trials for Congenital Heart Disease

Molecular and Cellular Characterization of Cardiac Tissue in Postnatal Development

Start date: April 2005
Phase:
Study type: Observational

The study team will use small pieces of human hearts which are removed as part of a required surgical procedure to study different objectives. One of the objective is how calcium ions pass through the membrane of heart cells in order to tell the heart cell how much force to contract with when the heart beats. Investigators will also study the proteins and RNA of these pieces to determine how the newborn heart cells control their force of contraction differently from adult heart cells. Investigators hypothesize that infant hearts have different regulation of calcium entry than adult hearts. The study team also wants to study combinations of 3D cardiac spheres with multiple environmental cues that can improve functional and metabolic maturation of Human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) and generate a more clinically relevant cell model.

NCT ID: NCT00238810 Completed - Clinical trials for Congenital Heart Disease

Relationship of Brain Natriuretic Peptide (BNP) Levels to Cardiac Diagnosis, Operation Performed, Post-operative Course and Outcome

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

The purpose of this study is to assess brain natriuretic peptide levels to evaluate the relationship of those levels with the diagnosis of congenital cardiac disease, operation performed, post-operative course, and outcome.

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: NCT00215085 Terminated - Clinical trials for Congenital Heart Disease

Cardiac Tumors in Children

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

The purpose of this study is to define the natural history of untreated cardiac tumors, study the pathology of primary cardiac tumors, review the surgical treatment and results of primary cardiac tumors and to determine the prognosis for these tumors.