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Congenital Heart Disease clinical trials

View clinical trials related to Congenital Heart Disease.

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NCT ID: NCT03156764 Terminated - Clinical trials for Congenital Heart Disease

Qp/Qs Ratio by Noninvasive Methods in Children With Shunt Dependent Pulmonary Circulation

Start date: May 23, 2017
Phase:
Study type: Observational

In pediatric cardiac patients with shunt dependent pulmonary circulation, Qp/Qs ratio is a important parameter indicating the balance of pulmonaty and systemic circulation. This study will calculate Qp/Qs using variables measured using non-invasive monitors (cerebral oximeter and pulse oximeter). This value will be compared with Qp/Qs calculated using variables obtained from blood sample.

NCT ID: NCT02769624 Terminated - Clinical trials for Congenital Heart Disease

Acute Effects of Inhaled Treprostinil in Fontan Patients

Start date: February 21, 2017
Phase: Phase 2
Study type: Interventional

In this pilot study investigators propose to explore the effects of a locally delivered inhaled pulmonary vasodilator (inhaled treprostinil) on exercise performance, pulmonary blood flow, venous pressure response and vascular function in stable Fontan patients. Investigators will also assess the effects of resting and acute rises in exercise induced systemic venous pressure on liver stiffness and will also assess whether treprostinil will attenuate the acute stiffness increase that investigators expect to see. This will be a prospective, randomized, double-blinded placebo controlled, crossover trial. Following recruitment and informed consent, each participant will undergo three study visits, including baseline testing (visit 1), followed by two sets of exercise and vascular function tests (visit 2 and visit 3) at CCHMC. Twenty-six patients will be enrolled in this study.

NCT ID: NCT02564796 Terminated - Anemia Clinical Trials

Erythropoietin to Prevent Unnecessary Transfusions In Patients With Cyanotic CHD - A Prospective Control Trial

Start date: November 2016
Phase: Phase 2
Study type: Interventional

Cyanotic congenital cardiac patients require higher hemoglobin concentrations (red blood cell levels) for optimal oxygen delivery to the body. Prophylactic erythropoietin (EPO) and iron can prevent and/or decrease the amount of blood transfusions needed in this population. We seek to investigate if EPO and iron make a clinically significant difference in the number of transfusions given to these patients and the morbidity associated with it.

NCT ID: NCT02551107 Terminated - Clinical trials for Congenital Heart Disease

Infant Nasal Nitric Oxide Levels in Congenital Heart Disease

Start date: December 2015
Phase: N/A
Study type: Interventional

This pilot study aims to measure nasal nitric oxide (nNO) in a group of neonates and infants (≤ 12 months) with congenital heart disease (CHD) and compare their nNO levels to age matched controls without CHD. CHD patients will be divided into subgroups, based on their cardiac anatomy, to try and identify a level of risk of ciliary dyskinesia within the subgroup of CHD. Each of these sub groups' nNO levels will be compared between groups and against age matched control infants without CHD.

NCT ID: NCT02408848 Terminated - Clinical trials for Congenital Heart Disease

The Value of Three Dimensional Echocardiography in Congenital Cardiac Surgery

Start date: March 2015
Phase:
Study type: Observational

There are few studies evaluating the value of 3D echocardiography in children undergoing congenital cardiac surgery. The aim of this observational study is to describe common and uncommon congenital malformations with the help of 3D echo and compare the findings and the measurements with those obtained with conventional 2D echo.

NCT ID: NCT02060825 Terminated - Clinical trials for Congenital Heart Disease

The Use of Optical Oximetry in Determining Gastrointestinal Complications After the Hybrid Procedure

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

This project is evaluating the validity of regional saturation monitoring in evaluating changes in the mesenteric perfusion. Regional saturation monitoring is a standard of care in many institutions, including NCH. Advances in the technology and recent approval of the use of CASMED devices for this purpose will allow us to use this technology more effectively. We aim to evaluate if there is a change in the mesenteric blood flow during the pre, intra and post operative period for the hybrid procedure and the balloon atrial septostomy procedure (BAS).

NCT ID: NCT02046135 Terminated - Acute Kidney Injury Clinical Trials

Sodium Bicarbonate to Prevent Acute Kidney Injury in Children Undergoing Cardiac Surgery

Start date: September 2013
Phase: Phase 2
Study type: Interventional

The proposed study will investigate the effect of sodium bicarbonate on the prevention of acute kidney injury in children undergoing cardiac surgery with cardio-pulmonary bypass. The investigators hypothesize that the occurrence of acute kidney injury will be less in children treated with sodium bicarbonate in the perioperative period when compared to placebo. The specific aims of this proposal are as follows: 1. To institute a prospective, randomized, double-blinded, placebo-controlled trial in pediatric subjects undergoing cardiac surgery to determine the efficacy of sodium bicarbonate on prevention of acute kidney injury as measured by pRIFLE criteria. 2. To examine whether treatment with sodium bicarbonate modifies the duration of acute kidney injury, fluid balance, hospital length of stay, need for dialysis, and progression to kidney failure. 3. To determine the relevance of NGAL as a biomarker to predict development of acute kidney injury.

NCT ID: NCT02004756 Terminated - Clinical trials for Congenital Heart Disease

Mechanisms of Dysfunction and the Influence of Exercise on Cardiac and Musculoskeletal Function

Start date: January 2010
Phase: Phase 1/Phase 2
Study type: Interventional

Primary Objective: To determine if impairments in cardiac and musculoskeletal function and metabolism exist in Fontan children. Secondary Objectives: 1. To determine if impairments do exist, are they related to exercise capacity. 2. To determine if a 12-week exercise training intervention improves cardiac and/or musculoskeletal metabolism. Hypothesis: The investigators hypothesize that abnormalities in cardiac and skeletal function are evident, influence exercise capacity, and can be improved with exercise training.

NCT ID: NCT01698567 Terminated - Clinical trials for Congenital Heart Disease

Antithrombin III in Infants With Cardiopulmonary Bypass (CPB)

Start date: July 2012
Phase: Phase 1
Study type: Interventional

The purpose of this study is to discern whether supplementation of Antithrombin III will decrease coagulation and inflammation associated with cardiopulmonary bypass in infants undergoing cardiac surgery.

NCT ID: NCT01639937 Terminated - Clinical trials for Congenital Heart Disease

Myocardial Perfusion and Scarring in Congenital Heart Disease

Start date: October 24, 2012
Phase:
Study type: Observational

Background: - People with congenital heart disease may develop heart failure earlier that those who do not have the disease. One theory to explain this is that the heart s own blood supply may be different in people with congenital heart disease. Problems with this blood supply can severely damage the heart. This damage can be studied with a heart imaging test called a cardiac magnetic resonance imaging (MRI) scan. Researchers want to use this type of scan to look at the blood supply to the heart in people with congenital heart disease. Objectives: - To learn more about the blood supply to the heart in people with congenital heart disease. Eligibility: - Individuals at least 18 years of age who have heart defects caused by congenital heart disease. Design: - Participants will be screened with a physical exam and medical history. Blood and urine samples will be collected. - Participants will have a cardiac MRI scan to look at the blood flow to the heart. - Participants will also have a heart stress test to measure heart function during exercise. - Other imaging studies of the heart may be performed to collect more information on heart function.