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Congenital Abnormalities clinical trials

View clinical trials related to Congenital Abnormalities.

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NCT ID: NCT00462462 Completed - Clinical trials for Congenital Venous Malformation

Systemic and Local Diffusion of Ethanol After Administration of Ethanol 96% Formulated in a Gel and Ethanol 98% Solution by the Percutaneous Route, in Patients With Congenital Venous Malformations:Pharmacokinetic, Pharmacodynamic and Clinical Study.

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

Absolute ethanol has been used "off-label" as an unmodified formulation (solution) in Congenital Venous Malformations (CVM). Despite its effectiveness, absolute ethanol appears difficult to handle because of its high diffusion capacity outside the CVM and in the blood circulation. A less diffusible ethanol-based product (ethanol gel) has been developed in order to minimize systemic and local diffusion capacities of ethanol. Therefore, the pharmacokinetic parameters and their clinical and paraclinical outcomes between ethanol gel 96% and absolute ethanol need to be carried out. FDA Office of Orphan Products Development (FDA OOPD) : Funding source.

NCT ID: NCT00443599 Completed - Hyperglycemia Clinical Trials

SPECS: Safe Pediatric Euglycemia in Cardiac Surgery

SPECS
Start date: November 2006
Phase: N/A
Study type: Interventional

Critically ill children, including children undergoing heart surgery, commonly develop elevated blood glucose (also known as "blood sugar") levels during their illness, which can lead to poor health outcomes and an increased risk of death. This study will examine the effectiveness of maintaining normal blood glucose levels at decreasing infections and improving recovery in young children undergoing heart surgery.

NCT ID: NCT00412035 Completed - Clinical trials for Unequal Length of Limbs; Congenital

Botox Injection for Lower Extremity Lengthening and Deformity Correction Surgery

BOLLD
Start date: January 2007
Phase: Phase 3
Study type: Interventional

The purpose of this six site multi-center study is to determine if BTX-A can alleviate the post-operative pain and improve the functional and quality of life outcomes of children with limb length discrepancy or angular deformity undergoing limb lengthening or deformity correction.

NCT ID: NCT00409708 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder

Effects of Methylphenidate on Cellular Abnormalities in Children With Attention Deficit Hyperactivity Disorder (ADHD)

Start date: November 2006
Phase: Phase 2
Study type: Interventional

This study will assess the frequency of chromosomal abnormalities measured in circulating lymphocytes in treatment-naive children with Attention Deficit Hyperactivity Disorder (ADHD) treated for 3 months with either extended release methylphenidate or behavioral therapy.

NCT ID: NCT00396877 Completed - Clinical trials for Heart Defects, Congenital

Efficacy And Safety Of Clopidogrel In Neonates /Infants With Systemic To Pulmonary Artery Shunt Palliation

CLARINET
Start date: November 2006
Phase: Phase 3
Study type: Interventional

Contemporary management of cyanotic congenital heart disease includes three stages of surgery. Incidence of shunt thrombosis and death between the two first stages of palliation remains important. The primary objective of the study is to evaluate the efficacy of Clopidogrel 0.2 mg/kg/day for the reduction of all cause mortality and shunt related morbidity in neonates or infants with cyanotic congenital heart disease palliated with a systemic-to-pulmonary artery shunt (e.g. modified Blalock Taussig Shunt [BTS]). The secondary objective was to assess the safety of Clopidogrel in the study population.

NCT ID: NCT00389935 Completed - Clinical trials for Hereditary Hemorrhagic Telangiectasia

Thalidomide Reduces Arteriovenous Malformation Related Gastrointestinal Bleeding

TAG
Start date: October 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether Thalidomide is effective in the treatment of arteriovenous malformations in the gastrointestinal tract.

NCT ID: NCT00389181 Completed - Clinical trials for Arteriovenous Malformations, Cerebral

A Randomized Trial of Unruptured Brain AVMs

ARUBA
Start date: October 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if medical management is better than invasive therapy for improving the long-term outcome of patients with unruptured brain arteriovenous malformations.

NCT ID: NCT00371891 Completed - Clinical trials for Coronary Arteriosclerosis

Ontario Multidetector Computed Tomographic (MDCT) Coronary Angiography Study (OMCAS)

Start date: September 2006
Phase: Phase 4
Study type: Interventional

Multidetector Computed Tomographic Coronary Angiography (MDCTCA) has been recently demonstrated to be accurate and may be used as a potential alternative to conventional invasive coronary angiography, which requires cardiac catheterization, for the diagnosis of coronary artery disease. The purpose of this study is to see if MDCTCA can identify significant coronary artery disease as good as or better than conventional coronary angiography (CICA). The study is designed to enroll 900 subjects and is being conducted in 6 hospitals in Ontario. Subjects scheduled for conventional cardiac catheterization and coronary angiography will receive an additional test using MDCTCA. The information gathered during the MDCTCA will be compared to the results of the scheduled conventional invasive coronary angiogram.

NCT ID: NCT00368732 Completed - Clinical trials for Heart Defects, Congenital

Genetic and Nutritional Causes of Heart Birth Defects

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

Each year in the United States, thousands of babies are born with heart defects. Women who take folic acid during pregnancy have a lower risk of giving birth to infants with heart defects, but the reason for this remains unknown. This study will examine the relationship between genes, nutrition, and the occurrence of heart defects in infants.

NCT ID: NCT00363363 Completed - Clinical trials for Heart Defects, Congenital

Physical Activity in Fontan Patients

Start date: August 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine which is the most effective intervention for increasing lifestyle physical activity in Fontan patients: an education (stage of change) intervention or a physical activity (mastery experience) intervention.