Clinical Trials Logo

Congenital Disorders clinical trials

View clinical trials related to Congenital Disorders.

Filter by:

NCT ID: NCT00327951 Terminated - Clinical trials for Congenital Disorders

Infant Weight Gain With Trisomy 21 and CAVC

Start date: January 2001
Phase: N/A
Study type: Observational

Failure to thrive and difficulty gaining weight is a sign of uncompensated congestive heart failure (CHF). Infants with Trisomy 21 and complete atrioventricular canal defects (CAVC) frequently develop uncompensated CHF and weight gain failure pre-operatively. A weight of 5 kg has been suggested as optimal for timing of CAVC repair. A delay in surgical repair often occurs if weight gain stalls and reaches a plateau prior to reaching 5 kg. A retrospective review performed by Kogon, et al, of children undergoing surgery for VSD at CHOA at Egleston recently reported that age and weight at surgery may not, however, be associated with adverse surgical outcome. The purpose of this study is to determine the optimal timing for surgical correction of CAVC in Trisomy 21 infants based on reaching a plateau of failed weight gain despite maximal anti-congestive and nutritional therapy.

NCT ID: NCT00327899 Terminated - Clinical trials for Congenital Disorders

Home Inotropic Therapy in Children

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

Inotropic therapy is a well-established practice for children with advanced congestive heart failure (CHF). Inotropes are intravenous medications to help the heart pump stronger and prolong life while awaiting heart transplantation. Traditionally children have been maintained on inotropic therapy in the hospital under close, monitored supervision. The United Network for Organ Sharing (UNOS), which governs organ distribution, has now changed listing criteria allowing patients awaiting heart transplantation to be discharged to home, yet maintaining a higher status on the waiting list. In adults, home inotropic therapy has been shown to be a safe and cost-effective bridge to transplantation. To date, there are no data on the use of home inotropic therapy in children. Hypothesis: We request to do a retrospective chart review of patients receiving this therapy to determine safety and efficacy of continuous ambulatory home inotropic therapy in children.

NCT ID: NCT00327886 Terminated - Clinical trials for Congenital Disorders

Managing Cyanosis Following Bidirectional Glenn Operation

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

The purpose of this retrospective study is to review the postoperative medical management of infants who underwent bidirectional Glenn operation from January 1, 2003 to December 31, 2005 who were significantly cyanotic.

NCT ID: NCT00327782 Terminated - Clinical trials for Congenital Disorders

Palliative Care of Children With End-Stage Heart Failure

Start date: January 1995
Phase: N/A
Study type: Observational

Palliative care in pediatric oncology and neurology is well described in the literature. There is a lack of information on the care of children terminally ill due to heart failure. A significant number of children are diagnosed with terminal heart failure for which palliative care is required. Objective: To describe palliative care of children over one year of age with end-stage heart failure, including need for and types of pain control, hospice use, need for and use of home nursing and quality of life issues.

NCT ID: NCT00277992 Terminated - Clinical trials for Congenital Disorders

Growth in Children With HLHS

Start date: January 2001
Phase: N/A
Study type: Observational

Children with HLHS have a history of poor enteral intake and growth. Over the past several years a modification to the Norwood operation was instituted (RV to PA shunt in place of the standard Blalock-Taussig shunt). The purpose of this study is to evaluate whether children who underwent this modification of the Norwood procedure had improved growth compared to those in past years who underwent traditional Norwood.

NCT ID: NCT00277979 Terminated - Clinical trials for Congenital Disorders

3D Echocardiography Managing Infantile Pompe's Disease

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

Pompe's disease, also known as glycogen storage disease type II, is a genetic disorder due to deficiency of acid glucosidase (GAA), which results in lysosomal glycogen storage in various tissues. Very low levels of GAA usually present in infancy, lead to a progressive cardiac and skeletal muscle disorder and death before age 1 year. Most infants develop massive hypertrophic cardiomyopathy which progresses to dilated cardiomyopathy and cardiorespiratory arrest. 3D echocardiography can be a simple, non-invasive method of following cardiac disease progression in infantile Pompe's disease.

NCT ID: NCT00277953 Terminated - Clinical trials for Congenital Disorders

MRI Review of Tracheal Dimensions

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

To date, there have been no published reports of normal variations in tracheal dimensions for pediatric patients undergoing MRIs. While there are reports of normals in CT studies, the reported dimensions were for average areas and lengths over the entire length of the trachea and not for normal variation in the dimensions at various sites in the trachea. Moreover, CT measurements are likely not entirely applicable to MRI measurements. Since cardiac MRI has become the procedure of choice to document the presence of vascular rings as well as the significance of any ring that is found, there is a need for normal values to be generated. This would in turn permit physicians to determine in cases of documented vascular rings the severity of the tracheal stenosis/deformity if found.

NCT ID: NCT00277940 Terminated - Clinical trials for Congenital Disorders

Aortic Arch Reconstruction

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

Abnormalities of the aorta have been identified in patients who have undergone repair of coarctation of the aorta by various surgical techniques. These abnormalities are thought to contribute to ventricular hypertrophy, hypertension and exercise intolerance. Aortic arch reconstruction is performed for a variety of lesions besides simple coarctation of the aorta; these include hypoplastic left heart syndrome and its variants. In the latter group of patients extensive reconstruction is performed usually with a pulmonary homograft. We have previously shown that the neo-aortic dimensions and geometry are abnormal. The elastic properties of the neo-aorta, however, have not previously been described.

NCT ID: NCT00277927 Terminated - Clinical trials for Congenital Disorders

Mild Valvar Pulmonary Stenosis

Start date: January 1984
Phase: N/A
Study type: Observational

Mild valvar pulmonary stenosis can be detected in 1/10,000 live births. Historical data suggested that most of these patients do well. Nonetheless, the majority of these patients is followed periodically by a pediatric cardiologist and may undergo repeated echocardiographic studies to follow the gradient. Such follow-up can be costly and it is not know if there is any benefit to periodic evaluation.

NCT ID: NCT00268112 Terminated - Clinical trials for Congenital Disorders

Resynchronization of Left Ventricular Contraction After Reimplantation of Anomalous Left Coronary Artery

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

Spontaneous resynchronization of dyskinetic segments of the left ventricle occurs after coronary bypass surgery in adults and has been shown in some children. It is, however, unknown what degree of dyskinesis is likely to be reversible in infants with ischemia from anomalous coronary arteries and what criteria would indicate that a resynchronization strategy of biventricular pacing might be needed. These questions need data from quantitative serial tissue Doppler observations of patients from pre-operative to late post-operative follow-up.