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Tricuspid Atresia clinical trials

View clinical trials related to Tricuspid Atresia.

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NCT ID: NCT01292551 Completed - Clinical trials for Hypoplastic Left Heart Syndrome

Study of Placebo or Bosentan to Treat Patients With Single Ventricle Physiology.

TEMPO
Start date: February 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether Bosentan is an effective and safe treatment to adolescent and adult (15 years and older) patients, born with one ventricle of the heart instead of two (single ventricle physiology) and who have undergone TCPC as a palliative surgical treatment. The aim of the TCPC operation is to use the one functioning ventricle to pump the blood flow to the body, while the blood to the lungs is received directly from the caval veins, and is thus a passive flow, without the aid of a ventricle to actively pump the blood through the pulmonary circulation. The resistance in the pulmonary circulation is therefore critical to these patients. These patients have markedly lower work capacity in bicycle test than the general public. Furthermore they have a high risk of developing complications e.g. loss of protein from the intestines. Bosentan is a medication that lowers the resistance in the pulmonary circulation. It is routinely used for patients with pulmonary hypertension. Some studies have shown that drugs that lower the pulmonary resistance can increase exercise capacity significantly in patients with single ventricle physiology. In this study 80 patients will receive either placebo or Bosentan for 14 weeks. Before and after the treatment, bicycle test along with blood samples, stool samples and quality of life interviews will be performed. Every four weeks during the study blood samples, physical exam and interviews will be performed to ensure the safety of the treatment. The investigators expect to find a significant increase in work capacity after 14 weeks in the treatment group compared with the placebo group. Moreover the investigators hope to find a decrease in intestinal protein loss and an improved quality of life.

NCT ID: NCT00974025 Completed - Clinical trials for Hypoplastic Left Heart Syndrome

Impact of Vitamin C on Endothelial Function and Exercise Capacity in Fontan-Palliated Patients

Start date: June 2009
Phase: N/A
Study type: Interventional

In this study, investigators will evaluate the effect of vitamin C on endothelial function, exercise tolerance and quality of life in patients with a single ventricle who have been palliated to Fontan physiology. The hypothesis is that vitamin C will result in improved exercise tolerance and endothelial function in patients who have undergone the Fontan operation, compared to placebo.

NCT ID: NCT00573066 Completed - Tetralogy of Fallot Clinical Trials

Understanding Dexmedetomidine In Infants Post-Operative From Cardiac Surgery

InfantDex
Start date: May 2004
Phase: Phase 1
Study type: Interventional

This study is being conducted to determine what dexmedetomidine does to the body and in turn, what how the body handles the medication. This medication, for the purpose of this trial, is used as a short-term sedative for infants who are immediately post-operative from cardiac surgery and have a breathing tube and are breathing with the assistance of a mechanical ventilator or breathing machine.

NCT ID: NCT00571233 Completed - Clinical trials for Hypoplastic Left Heart Syndrome

Biomarker Study for Heart Failure in Children With Single Ventricle Physiology

BHFSVP
Start date: February 2007
Phase: N/A
Study type: Observational

The purpose of this study is to determine if children with heart disease where there is only one pumping chamber("ventricle") have proteins (biomarkers") in the blood that can be used to monitor the function of their heart.

NCT ID: NCT00507819 Completed - Clinical trials for Hypoplastic Left Heart Syndrome

Sildenafil After the Fontan Operation

SAFO
Start date: December 2007
Phase: Phase 2
Study type: Interventional

In this study, the investigators will evaluate the effect of sildenafil on exercise tolerance in patients with a single cardiac ventricle who have undergone the Fontan operation. The investigators will also evaluate echocardiographic measures of ventricular function and measure quality of life changes using two validated quality of life measures. The hypothesis is that sildenafil will result in increased exercise tolerance in patients who have had the Fontan operation as compared to placebo.

NCT ID: NCT00004828 Completed - Clinical trials for Heart Defects, Congenital

Liothyronine in Children With Single Ventricle Congenital Cardiac Malformations Undergoing the Fontan Procedure

Start date: December 1994
Phase: Phase 1
Study type: Interventional

OBJECTIVES: I. Determine the pharmacokinetics of exogenous liothyronine administered in children undergoing the modified Fontan procedure. II. Determine the liothyronine supplementation dose that counters the fall in serum liothyronine concentrations and provides the greatest potential myocardial benefit after the modified Fontan procedure. III. Evaluate the potential toxicity of exogenous liothyronine administered in children undergoing a modified Fontan procedure.