RecruitingNCT06969924

Real-World Data on the Effects of Cardiac Resynchronization Therapy in Adult Patients With Congenital Heart Disease

Sponsor

Leiden University Medical Center

Enrollment

100 participants

Start Date

Jan 1, 2014

Study Type

OBSERVATIONAL

Conditions

Adult Congenital Heart Disease

Summary

This study aims to evaluate the real-world effects of cardiac resynchronization therapy (CRT) in adult patients with congenital heart disease (ACHD). Specifically, it seeks to determine whether CRT improves clinical outcomes in this unique patient population and to identify factors associated with a favorable response to therapy.

Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is collecting real-world data on how cardiac resynchronization therapy (CRT) — a special type of pacemaker that helps the heart's chambers beat in a more coordinated way — works in adults who were born with heart defects (congenital heart disease). **You may be eligible if...** - You are an adult (18 or older at the time of device implantation) - You have congenital heart disease - You have already had a CRT device implanted **You may NOT be eligible if...** - You were under 18 years old when your CRT was implanted - You object to your retrospective medical data being used in research Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICECardiac resynchronization therapy

Cardiac resynchronization therapy pacemaker or defibrillator with a transvenous or epicardial systemic ventricle lead

Locations(1)

Leiden University Medical Center (LUMC)

Leiden, South Holland, Netherlands

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NCT06969924

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