MRI Evaluation of Atrial Scar Tissue Using Gadolinium in Patients Aged 13 and Older with Repaired Congenital Heart Disease
Led by Boston Children's Hospital · Updated on 2025-02-13
50
Participants Needed
1
Research Sites
156 weeks
Total Duration
AI-Summary
What this Trial Is About
This research focuses on patients aged 13 and older with congenital heart disease who have undergone surgical repair and may develop atrial arrhythmias such as intra-atrial reentrant tachycardia and atrial fibrillation. The study aims to better understand how well scar tissue in the hearts atria can be seen using cardiac MRI with a contrast agent called gadolinium. Researchers want to learn how these MRI findings relate to measurements taken during procedures in the electrophysiology laboratory.
Participants will have cardiac MRI scans as part of their usual medical care, involving the use of gadolinium contrast to visualize scar tissue in the hearts atria. The study will analyze 3D late gadolinium enhancement images to quantify atrial fibrosis and compare these findings with voltage maps obtained during electrophysiology procedures. This imaging technique is being evaluated for its reproducibility and potential to provide insight into heart tissue changes in patients with repaired congenital heart disease.
During the study, participants will undergo cardiac MRI scans and may have electrophysiology laboratory evaluations as part of their routine care. Researchers will measure total atrial fibrosis using 3D late gadolinium enhancement MRI over one year and compare it with voltage mapping results over two years. They will also track occurrences of sustained atrial arrhythmias lasting more than 30 seconds over five years using ECG and monitoring methods. The study is observational and focuses on collecting detailed imaging and clinical data to better understand heart scarring in this population.
CONDITIONS
Brief Title
Atrial Late Gadolinium Enhancement in Patients with Repaired Congenital Heart Disease
Research Team
D
Daniel A Castellanos, MD
E
Edward O'Leary, MD
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Patients older than 13 years with congenital heart disease
Referred for cardiac MRI and receiving gadolinium contrast as part of routine clinical care or for pre-ablation planning
You will not qualify if you...
Self-reported anxiety or claustrophobia
Presence of a permanent pacemaker or implantable cardioverter defibrillator
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Diagnostic Evaluation
Duration - 1 day
Participants undergo a cardiac MRI with gadolinium contrast to take pictures of the atria and identify scar tissue.
1 visit (in-person)
Long-term Monitoring
Duration - Up to 5 years
Participants are observed over several years to assess atrial fibrosis and monitor for sustained atrial arrhythmias.
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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Published Research Related To This Trial
Three-Dimensional Late Gadolinium Enhancement Cardiovascular Magnetic Resonance Predicts Inducibility of Ventricular Tachycardia in Adults With Repaired Tetralogy of Fallot.
Association of atrial fibrosis quantified using LGE-MRI with atrial appendage thrombus and spontaneous contrast on transesophageal echocardiography in patients with atrial fibrillation.