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A Phase III, Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Efficacy of Tadalafil Versus Placebo in Improving Hemodynamics and End-Organ Dysfunction in Fontan Physiology (TRIUMPH Trial) (TRIUMPH)
Rochester, Minn.
The primary study objectives are to examine the therapeutic potential of Tadalafil in improving endothelial function, hemodynamic capabilities, and end-organ function in patients who have previously undergone a Fontan Palliation.
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Cardiac MRI in Patients with Congenital Heart Disease
Rochester, Minn.
The purpose of this study is to create a standardized cardiac MRI imaging protocol for patients with Congenital Heart Disease.
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Control Population for the Mayo Clinic Adult Congenital Heart Disease Registry
Rochester, Minn.
The purpose of this study is to provide all studies that contribute to the Mayo Clinic Adult Congenital Heart Disease (MACHD) Registry with a control cohort, this study will combine all testing needed for each of the studies.
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Invasive Hemodynamic Control Cohort for The Mayo Clinic Adult Congenital Heart Disease (MACHD) Registry
Rochester, Minn.
The purpose of this study is to assess invasive hemodynamic indices at rest and during supine cycling exercise in healthy patients.
These will serve as healthy controls and will be used for comparisons in the analysis of data from the Mayo Clinic Adult Congenital Heart Disease Registry (MACHD Registry).
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Pathophysiologic Mechanism for Arrhythmias and Impaired Aerobic Capacity in Tetralogy of Fallot & Other Congenital Heart Diseases
Rochester, Minn.
The purpose of this study is to explain the functional change mechanism linking right atrial (RA) hypertension, right heart (RH) remodeling and onset of symptoms such as arrhythmias and impaired aerobic capacity, since symptomatic status is a risk factor for mortality in the Tetralogy of Fallot (TOF) population.
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Role of Biomarkers in Risk Stratification in Adults with Congenital Heart Disease: The ACHD Biobank Project
Rochester, Minn.
The purporse of this study is to determine if biomarker assay obtained at baseline can predict future risk of cardiovascular adverse events, and to determine if temporal changes in biomarker levels can provide a better risk prediction compared to biomarker assay obtained at baseline.
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