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Heart Defects, Congenital clinical trials

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NCT ID: NCT01693796 Completed - Clinical trials for Cardiac Catheterizations

Evaluation of Thyroid Exposure to Radiation Doses During Paediatric Cardiac Catheterisations Performed for Diagnosis or the Treatment of Congenital Heart Disease

Start date: March 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the average risk for thyroid irradiation for any type of paediatric cardiac catheterization, based on the cummulative at-risk dose of 100 mSv, adjusted to the measured thyroid volume and to the patient's age.

NCT ID: NCT01679275 Completed - Clinical trials for Heart Defects, Congenital

Pre-operative Cerebral Oxygenation in Neonates With Congenital Heart Disease

CHD-NIRS
Start date: October 2012
Phase:
Study type: Observational

Congenital heart disease with need for early surgery in newborns is associated with an increased incidence in global impairment in development. The causes of these late adverse neurologic outcomes are multifactoral and include both fixed (or patient-specific factors) and modifiable factors. They relate to both the mechanism of central nervous system injury associated with congenital heart disease and its treatment. Measuring cerebral oxygenation is a promising non-invasive way of cerebral monitoring in a neonatal intensive care unit. The importance of cerebral monitoring in neonates with congenital heart problems at risk of developing neurological complications is increasingly recognized. In this way the most vulnerable moments for the newborn brain can be detected and ,if possible, lead to change in (timing of) treatment.

NCT ID: NCT01671566 Completed - Clinical trials for Congenital Heart Defects

Interval Training in Adults With Congenital Heart Disease a Randomized Trial

Start date: September 2012
Phase: N/A
Study type: Interventional

Adults with congenital heart disease have various degrees of impaired exercise capacity compared to healthy controls. Impaired exercise capacity makes everyday activities more difficult and demanding. There are few studies on effect of exercise training in adults with congenital heart disease. The hypothesis of this study is that structured home based exercise training will improve exercise capacity and health status in the studied population.

NCT ID: NCT01669057 Completed - Clinical trials for Congenital Heart Disease

Study on Clinical Prognosis, Risk Factors and Genetic Basis of Congenital Heart Disease

SCPRFGBCHD
Start date: October 2011
Phase: N/A
Study type: Observational

The objective of this study is to investigate the effect of parental peri-natal environmental risk factors and genetic factors on the development of Congenital Heart Disease (CHD). Our hypothesis is that the distributions of some environmental and genetic risk factors significantly differ between neonates with and without CHD.

NCT ID: NCT01665261 Completed - Clinical trials for Congenital Heart Disease

Newborn Screening for Congenital Heart Disease

NSCHD
Start date: July 2012
Phase: N/A
Study type: Observational

The purpose of this study is to test the accuracy of 7 indicators in screening congenital heart defects (CHD) in all newborns (symptomatic or asymptomatic) to determine whether these indicators could be applied in the nationwide newborn CHD screening. The investigator's hypothesis is that 7 indicators are effective in neonate CHD screening with the acceptable accuracy.

NCT ID: NCT01662037 Completed - Clinical trials for Congenital Heart Defects

Bosentan Therapy in Children With Functional Single Ventricle

Start date: January 2010
Phase: Phase 2
Study type: Interventional

Bosentan is a kind of dual endothelin receptor antagonist.The purpose of this study is to investigate if Bosentan therapy can modify the outcome of children with functional single ventricle.

NCT ID: NCT01659411 Completed - Clinical trials for Pulmonary Arterial Hypertension

Adult Congenital Heart Disease Registry (QuERI)

Start date: December 1, 2011
Phase:
Study type: Observational [Patient Registry]

Multi-center, observational, U.S.-based longitudinal program. Data will be collected prospectively for 3 years. Individual physician feedback will be provided on data collected with the purpose of improving the management of patients - quality enhancement research initiative (QuERI) process from adult patients enrolled with a history of repaired Congenital Heart Disease (CHD).

NCT ID: NCT01656941 Completed - Clinical trials for Congenital Heart Disease

Genetic Determinants of Congenital Heart Disease Outcomes

GECHO
Start date: March 2011
Phase:
Study type: Observational

The purpose of this study is to examine the role of genetic variation in the oxidative stress response on critical perioperative and short-term outcomes after neonatal heart surgery. The goals will be to determine 1) if the oxidative stress pathway is an important one for therapeutic intervention in neonates with severe congenital heart defects and 2) if variants in the oxidative response pathway can be used to identify patients at increased risk for adverse outcomes.

NCT ID: NCT01632813 Completed - Critical Illness Clinical Trials

Leuven Growing Into Deficit Follow-up Study

Leuven-GID
Start date: July 2012
Phase: N/A
Study type: Observational

The key objective of the Leuven growing-into-deficit (GID) follow-up-study is to test the hypothesis that children with a congenital heart disease (CHD) show more neurocognitive impairment at the second follow-up at 7 years old than at the first follow-up at the age of 4, compared to healthy controls.

NCT ID: NCT01616394 Completed - Clinical trials for Congenital Heart Disease

Postoperative Troponin in Children With Congenital Heart Disease

Start date: February 2012
Phase: N/A
Study type: Observational

The aim of the study is to evaluate the value of postoperative troponin in the prediction of mid term and long term mortality and morbidity in children with congenital heart disease undergoing cardiac surgery.