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Heart Septal Defects, Atrial clinical trials

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NCT ID: NCT00498446 Completed - Clinical trials for Atrial Septal Defect

Magnetic Resonance Imaging of Atrial Septal Defects

Start date: July 2002
Phase:
Study type: Observational

An atrial septal defect (ASD) is a hole in the heart that can lead to heart failure. Depending on the size and severity of the ASD, They can be treated during a heart catheterization with a special device that can permanently seal the ASD, but knowing the exact size and severity of the ASD is crucial. Newer MRI techniques may provide a better way at diagnosing the size and severity of an ASD. We compared MRI to other standard clinical ways for evaluating an ASD.

NCT ID: NCT00480740 Completed - Clinical trials for Atrial Septal Defect

The Pharmacology and Hemodynamics of Dexmedetomidine in Children With Congenital Heart Disease

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

The purpose of this study is to examine the pharmacokinetics, pharmacodynamics, and pharmacogenomics of dexmedetomidine in the following three pediatric patient populations: patients with bi-directional cavopulmonary anastomosis or a Fontan procedure, patients who have had a cardiac transplant, and patients with otherwise normal physiology who are undergoing closure of a patent ductus arteriosis or atrial septal defect.

NCT ID: NCT00478296 Completed - Clinical trials for Congenital Disorders

Pulmonary Hypertension in Trisomy 21 Patients

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

Evidence has shown poor outcome for adult patients with pre-operative pulmonary hypertension following closure of an atrial septal defect. Life-threatening pulmonary hypertensive crises may occur in these patients when they no longer have an atrial communication to decompress high right heart pressures. This concern has led some to advocate fenestrated patch closure of ASDs in patients with pulmonary hypertension with the prospect of a repeated procedure in order to close the fenestrations at a later date.

NCT ID: NCT00353509 Completed - Clinical trials for Atrial Septal Defects

Safety and Effectiveness Study of the Solysafe Septal Occluder

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

Prospective mono-center clinical study to evaluate the safety and effectiveness of an intracardiac septal closure device in patients with atrial septum defect (ASD)

NCT ID: NCT00207376 Completed - Clinical trials for Patent Foramen Ovale

Safety and Effectiveness Study of the Solysafe Septal Occluder in Patients With Atrial Septum Defect and Patent Foramen Ovale

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

This is a prospective multicenter clinical study to evaluate the safety and effectiveness of an intracardiac septal closure device in patients with atrial septum defect (ASD) and patent foramen ovale (PFO).

NCT ID: NCT00005546 Completed - Clinical trials for Cardiovascular Diseases

Molecular Genetic Epidemiology of Three Cardiac Defects -SCOR in Pediatric Cardiovascular Disease

Start date: January 1999
Phase: N/A
Study type: Observational

To identify genes involved in the pathogenesis of three types of congenital heart disease, atrial septal defects, paramembranous ventricular septal defects, and atrioventricular canal defects.

NCT ID: NCT00005322 Completed - Clinical trials for Cardiovascular Diseases

Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease

Start date: January 1990
Phase: N/A
Study type: Observational

To identify genes involved in the pathogenesis of congenital heart disease, including atrial septal defects (ASDs), paramembranous ventricular septal defects (VSDs), and atrioventricular canal defects (AVCDs).

NCT ID: NCT00005190 Completed - Clinical trials for Cardiovascular Diseases

Reproduction and Survival After Cardiac Defect Repair

Start date: July 1986
Phase: N/A
Study type: Observational

To create a registry of all Oregon children undergoing surgical repair of congenital heart disease since 1958 in order to determine mortality, morbidity, and disability after surgery and to assess the safety of pregnancy in women with corrected congenital heart disease and the risk of prematurity and occurrence of congenital heart defects in offspring.