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Single-ventricle clinical trials

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NCT ID: NCT03339466 Completed - Single-ventricle Clinical Trials

Inspiratory Muscle Therapy in Subjects With Fontan Circulations

Start date: January 29, 2016
Phase: N/A
Study type: Interventional

Individuals who have undergone the Fontan procedure are uniquely dependent upon respiratory mechanics to support pulmonary blood flow (PBF). The investigators hypothesized that enhanced respiratory muscle function via inspiratory muscle training (IMT) would improve performance on cardiopulmonary exercise stress testing (CPET).

NCT ID: NCT03322345 Enrolling by invitation - Clinical trials for Congenital Heart Disease

Characterizing the Effect of Dopamine on Markers of Lymph Re-circulation in Fontan-associated Protein-losing Enteropathy

Start date: April 9, 2019
Phase:
Study type: Observational

Patients that have undergone a Fontan procedure (surgical correction for single ventricle congenital heart disease) may develop a complication known as protein-losing enteropathy (PLE). Some studies suggest PLE is primarily caused by impaired lymph flow. Use of continuous dopamine infusion can improve PLE. Evidence suggests the effect of dopamine may be through its effect on lymphatic function. This observational study looks at markers of lymph flow and PLE symptoms after treatment using dopamine and other standard therapies during disease exacerbations.

NCT ID: NCT03263312 Active, not recruiting - Myocardial Fibrosis Clinical Trials

Multimodality Biomarkers for Noninvasive Assessment of the Fontan Patient

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

This is a single center prospective longitudinal exercise training study and will enroll approximately 50 Fontan patients and 20 controls of a similar age, gender, BMI and physical activity level between the ages of 10-40 years. Participants will undergo an MRI of the Fontan circulation. This will include imaging of the heart, lung and liver. This will include specific imaging for tissue characterization and assessment of myocardial fibrosis, liver fibrosis and disproportionate pulmonary blood flow. The investigators will then draw blood (approximately 10 ml) for assessment of serum biomarkers and circulating microRNAs of interest. The participants will undergo exercise testing and will then start a 3-6 month long cardiac rehabilitation program. After the 3-6 month study period the participants will return back for a follow up and repeat all the testing completed at enrollement.

NCT ID: NCT03119090 Completed - Clinical trials for Congenital Heart Disease

Fontan Imaging Biomarkers (FIB) Study

FIB
Start date: September 2015
Phase:
Study type: Observational

The goal of the Fontan Imaging Biomarkers (FIB) study is to identify the associations of blood and urine biomarkers to imaging parameters of ventricular mechanics.

NCT ID: NCT03088345 Completed - Clinical trials for Congenital Heart Disease

Early Use of Vasopressin in Post-Fontan Management

VAMP
Start date: March 6, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

This is an investigator initiated, prospective, single-center, double-blinded, randomized, placebo-controlled trial of post-operative low dose vasopressin infusions as an early treatment of low systemic perfusion in pediatric patients following Fontan palliation.

NCT ID: NCT02999438 Completed - Heart Failure Clinical Trials

Frailty in Children With Cardiac Disease

Start date: November 2016
Phase:
Study type: Observational

Frailty is a complex biologic syndrome of diminished physiologic reserve that leads to decreased resistance to stressors and is associated with adverse health outcomes. The syndrome has been well studied in adults and is quantified by the Fried criteria, which are comprised of five components- slowness, weakness, self-reported exhaustion, shrinkage and diminished physical activity. The concept of frailty is novel in children. A study in young adult childhood cancer survivors demonstrated increased incidence of frailty in this population along with increased risk of morbidity and mortality. This suggests that frailty as a phenotype has relevance outside of the geriatric age group. Pediatric patients with single ventricle physiology, heart failure and pulmonary artery hypertension- all represent populations with significantly increased risk of mortality, morbidity and decreased quality of life. Currently, such patients are monitored outpatient by serial echocardiograms and blood work that only gives information about end organ damage. But there is no validated tool available to measure global infirmity in such children. Better understanding of the relevance and applicability of frailty in pediatrics may allow for identification of the most vulnerable pediatric cardiac patients and be of value in optimizing their clinical management and improving health outcomes.

NCT ID: NCT02975999 Withdrawn - Pleural Effusion Clinical Trials

Use of Vasopressin Following the Fontan Operation

Start date: December 2016
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine whether Vasopressin following the Fontan operation will decrease chest tube output and duration.

NCT ID: NCT02946892 Completed - Single Ventricle Clinical Trials

Effect of Carvedilol on Exercise Performance in Fontan Patients

Start date: November 2016
Phase: Phase 4
Study type: Interventional

This study evaluates the effect of carvedilol in patients who have undergone a Fontan heart operation. All participants will receive carvedilol and placebo for 12 weeks. Exercise tests will be performed at the end of each 12 week period.

NCT ID: NCT02781922 Recruiting - Clinical trials for Hypoplastic Left Heart Syndrome

Cardiac Stem/Progenitor Cell Infusion in Univentricular Physiology (APOLLON Trial)

APOLLON
Start date: June 2016
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of intracoronary injection of JRM-001 after reconstructive surgery in pediatric patients with functional single ventricle

NCT ID: NCT02614664 Withdrawn - Clinical trials for Congenital Heart Disease

Changes in Cerebral Oxygenation During Laparoscopy in Patients With Single Ventricle Anatomy

Start date: November 2015
Phase:
Study type: Observational

Patients with single ventricle physiology (hypoplastic left heart syndrome, tricuspid atresia) frequently have feeding difficulties necessitating procedures such as Nissen fundoplication and G-tube placement. With advances in minimally invasive surgery, these are frequently performed using laparoscopic techniques. Although generally safe and effective, the increase in IAP during laparoscopy may increase systemic and pulmonary vascular resistance and decrease cardiac output. This prospective study will include 50 patients with single ventricle physiology presenting for laparoscopic procedures. There will be no change in the anesthetic or perioperative care of these patients. Tissue and cerebral oxygenation will be monitored using near infrared spectroscopy (NIRS).