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Congenital Heart Disease clinical trials

View clinical trials related to Congenital Heart Disease.

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NCT ID: NCT03119155 Recruiting - Clinical trials for Congenital Heart Disease

Improvement on Diagnosis of Fetal Congenital Heart Disease Based on Multi-center Collaboration in China

Start date: December 1, 2018
Phase:
Study type: Observational [Patient Registry]

The objective of this study is to improve the diagnosis level of fetal congenital heart disease by the multi-center collaboration in China.

NCT ID: NCT02996630 Recruiting - Clinical trials for Congenital Heart Disease

Assessing Neurodevelopment in Congenital Heart Disease.

NEUROHEART
Start date: May 2013
Phase: N/A
Study type: Interventional

Congenital heart disease (CHD) is the most prevalent congenital malformation affecting 1 in 100 newborns per year. Children with CHD are a known risk population for brain injury, with neurodevelopmental alterations shown over time in up to 50% of cases. No adequate description exists of the type of neurocognitive anomalies or risk factors associated with CHD, and consequently no prognostic markers that may allow identification of high-risk cases are available.

NCT ID: NCT02970071 Recruiting - Clinical trials for Congenital Heart Disease

The Application Value of STIC in the Diagnosis of Fetal Complex Congenital Heart Disease

STIC
Start date: April 25, 2017
Phase:
Study type: Observational

The objective of this study is to use of STIC technology to assist the traditional echocardiography to diagnose the fetal congenital heart disease accurately and then to provide a basis for prenatal counseling.

NCT ID: NCT02914392 Recruiting - Clinical trials for Congenital Heart Disease

Study on the Relationship Between Maternal Exposure to Environmental Factors and Fetal Congenital Heart Disease

Start date: May 18, 2017
Phase: N/A
Study type: Observational

The objective of this study is to research the relationship between maternal exposure to environmental factors and fetal congenital heart disease in a community-based case-control study.

NCT ID: NCT02897323 Recruiting - Clinical trials for Congenital Heart Disease

Northwest Adult Congenital Heart Disease Observatory

CARL
Start date: November 14, 2016
Phase: N/A
Study type: Observational

The incidence of congenital heart disease is about 8 per thousand live births. Thanks to advances in cardiac surgery, 90% of children born with heart defects reach adolescence and adulthood. Congenital heart defects are the leading cause of heart disease in young adults and expectant mothers in Western countries. The number of patients increases continuously as life expectancy increases. An increasing number of patients with complex heart defects survive to adulthood. The medico-surgical management of this highly specialized growing number of patients is difficult and requires a multidisciplinary collaboration. In France, an estimated 200,000 patients the number of carrier patients with congenital heart disease. Half of them will require monitoring, medical procedures, catheterizations and/or surgical re-intervention. No objective demographic data are currently available on the French patients. So, the investigators decided to set up an epidemiological project to better understand this cohort of patients. The main objective of this project is to obtain accurate epidemiological data needed to adapt the supply of care.

NCT ID: NCT02825472 Recruiting - Clinical trials for Congenital Heart Disease

Exercise Training in Grown-up Congenital Heart Disease

ExTra-GUCH
Start date: February 2016
Phase: N/A
Study type: Interventional

Rationale: Regular physical activity and aerobic exercise training are related to decreased cardiovascular mortality in healthy individuals, as well as in individuals with cardiovascular risk factors and cardiac patients. Unfortunately, no such data is available on exercise training in adult patients with congenital heart disease. Objective: The objective of the ExTra GUCH trial is to assess whether encouragement of a six-month sports participation program in addition to usual care in symptomatic adult patients with congenital heart disease improves exercise capacity and quality of life, and lowers serum N-terminal prohormone brain natriuretic peptide (NT-proBNP) levels. Study design: International, multi-centre parallel randomized controlled trial. Study population: Adult patients with congenital heart disease, who are in New York Heart Association (NYHA) class II or III. Intervention (if applicable): The intervention group receives a six-month individualized exercise training program, the control group receives usual care. Main study parameters/endpoints: The primary outcome is the change in peakVO2 between patients in the sports participation group, and the control group. Secondary outcome measures are change in NYHA functional class, quality of life, and NT-proBNP levels. The primary safety outcome is the composite of all hospitalizations, and all deaths during, or within three hours after exercise. The secondary safety outcome is the composite of all exercise related injuries for which medical attention is sought.

NCT ID: NCT02731248 Recruiting - Clinical trials for Congenital Heart Disease

Pulse Oximeter Screening in Congenital Heart Disease

POX
Start date: April 2016
Phase: N/A
Study type: Observational

Pulse oximetry screening of newborn infants increases early detection of critical congenital heart disease and minimises the risk of circulatory collapse before surgery. This study provides an update on the implementation of pulse oximetry screening in Turkey

NCT ID: NCT02618824 Recruiting - Clinical trials for Congenital Heart Disease

Role of Terminal Warm Blood Cardioplegia as Myocardial Protection in the Use of Histidine-Tryptophan-Ketoglutarate Cardioplegia in Complex Congenital Heart Surgery

Start date: December 2015
Phase: Phase 2
Study type: Interventional

Terminal warm blood cardioplegia (TWBC) has been shown to enhance myocardial protection in adult patients. Even in pediatric patients, the use of cold blood cardioplegia followed by administration of TWBC will provide cardioprotective effect similar to adult patients. Histidine-tryptophan-ketoglutarate (HTK), is attractive for cardiac surgeons because it is administered as a single dose and is claimed to offer myocardial protection for a period of up to 180 minutes allowing performance of complex procedures without interruption. Merging the use of TWBC on the use of HTK cardioplegia, especially for pediatric cardiac cases, have not been investigated. This technique is expected to provide a longer ischemic time and a protective effect against reperfusion injury.

NCT ID: NCT02414321 Recruiting - Clinical trials for Congenital Heart Disease

The Role of the Pulmonary Vasculature in the Fontan Circulation

Start date: June 2015
Phase:
Study type: Observational

This study aims to explore the structural and functional characteristics of the pulmonary vasculature in adult Fontan patients. Objectives: - Determine the effect of pulmonary vasodilatation on indexed cardiac output during simulated exercise. - Characterization of structural properties of small pulmonary arteries.

NCT ID: NCT02258724 Recruiting - Clinical trials for Congenital Heart Disease

Swiss National Registry of Grown up Congenital Heart Disease Patients

GUCH
Start date: September 2013
Phase:
Study type: Observational [Patient Registry]

Due to successes in the last decades in pediatric heart surgery and cardiology, 90-95% of the children with congenital heart disease reach adult age.This results in an increasing number of adults or "grown-ups" with congenital heart disease (ACHD or GUCH patients) that require special health care organization and training programmes. Long term complications of these GUCH patients and optimum treatment strategies are still poorly known. The aim of this registry is to collect quantitative and qualitative data regarding GUCH patients treated in specialised centres in Switzerland.