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Heart Defects, Congenital clinical trials

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NCT ID: NCT00543309 Terminated - Clinical trials for Heart Defects, Congenital

Effects of Perioperative Nesiritide or Milrinone Infusion on Recovery From Fontan Surgery

Start date: October 2007
Phase: Phase 2
Study type: Interventional

The staged surgical pathway to treat children with single ventricle heart defects culminates with the Fontan operation. In this procedure, systemic venous return is rerouted directly to the pulmonary arteries, which serves to separate the systemic and pulmonary circulations. Although mortality following the Fontan operation is now uncommon, early postoperative morbidity including prolonged postoperative chest tube drainage and hospitalization remains significant. The efficacy of empiric inotropic, vasodilator and neurohumoral-inhibitory therapies in the perioperative period is unknown and practice varies widely between centers. The investigators will propose a single-center, randomized, double-blind, phase II clinical trial in children undergoing Fontan surgery. The investigators plan to compare the effects of perioperative nesiritide, milrinone and placebo infusions on the early postoperative clinical course and neurohumoral profile. The investigators hypothesize that, when compared to the milrinone and placebo groups, the nesiritide group will have more days alive and out of the hospital within the first 30 days after surgery.

NCT ID: NCT00483951 Terminated - Clinical trials for Myocardial Infarction

Cardiovascular Disease Screening

Start date: January 28, 2008
Phase:
Study type: Observational

This study will evaluate volunteers 18 years of age and older to see if they qualify for one of NHLBI s research studies. Tests include the following: - General medical evaluation, which may include blood tests, chest x-ray, electrocardiogram (ECG) and echocardiogram (heart ultrasound). - Other tests as appropriate, such as magnetic resonance imaging (MRI), cardiac computed tomography (CT scan of the heart), nuclear stress test and echocardiography stress test. - X-ray contrast studies of the heart and blood vessels. (These may be excluded in patients with kidney risk factors.)

NCT ID: NCT00451698 Terminated - Clinical trials for Congenital Heart Defect

Erythropoietin and Pediatric Cardiac Surgery

EPO
Start date: October 2007
Phase: N/A
Study type: Interventional

Lack of bloodflow to the heart and brain when the heart is stopped during heart surgery can cause damage to those organs. We hypothesize that a single dose of erythropoietin prior to the heart bypass portion of surgery may protect the infant human heart and brain from injury. This randomized clinical trial will involve 120 children, age 6 weeks to 18 years, requiring heart bypass surgery for congenital heart defects.

NCT ID: NCT00359099 Terminated - Clinical trials for Congenital Heart Disease

Hepatitis C in Adults Who Underwent Congenital Heart Surgery Before Screening

Start date: January 1980
Phase: N/A
Study type: Observational

This is a retrospective chart review. We hypothesize that patients who have undergone congenital heart surgery, prior to screening of blood products have a significant risk of hepatitis C infection and all such patients would benefit from screening for hepatitis C.

NCT ID: NCT00335036 Terminated - Clinical trials for Congenital Heart Disease

Pediatric Lead Extractability and Survival Evaluation (PLEASE)

Start date: June 2006
Phase: N/A
Study type: Interventional

This is a randomized, prospective clinical trial comparing 2 different types of implantable cardioverter defibrillator (ICD) leads in children and patients with congenital heart disease. ICD lead survival in this patient group is particularly suboptimal, and lead extraction is technically difficult and carries a substantial morbidity risk. Recently, improved ICD lead designs have been released and are currently being utilized in patients. The main aim of the study is to determine if either type of lead performs better in terms of implantation electrical characteristics, long-term survival without breaking, and ease of extractability.

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: 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.

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.