VICTORY AF: Evaluation of Multielectrode Phased RF Technology in Persistent Atrial Fibrillation
Investigating Stroke Risk After Ablation Procedures
Brief description of study.
This study is a prospective, unblinded, multi-center, investigational, global, clinical study designed to evaluate the procedure and/or device related stroke rate within 30 days of an ablation procedure with the Medtronic Phased RF System.
Detailed description of study
This study is a prospective, unblinded, multi-center, investigational, global, clinical study designed to evaluate the procedure and/or device related stroke rate within 30 days of an ablation procedure with the Medtronic Phased RF System.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Atrial Fibrillation
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Age: 100 years or below
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Gender: All
This study investigates the risk of stroke within 30 days following an ablation procedure. An ablation is a medical procedure used to treat certain types of heart conditions by scarring or destroying tissue in the heart that is causing incorrect signals. The study aims to understand how often strokes occur after using an investigational system during these procedures.
Participants in this study will undergo an ablation procedure using a specific investigational system. The study will monitor and record any stroke events that occur within 30 days of the procedure to gather data on the safety and effectiveness of the system.
- Who can participate: Participants must be adults aged 18 and older with specific heart conditions eligible for ablation procedures. Other inclusion criteria may apply.
- Study details: Participants will undergo an ablation procedure using an investigational system. They will be monitored for any stroke events within 30 days post-procedure.
- Study Timelines: The study will last 30 days.
Interested in the study?
Select a study center that’s convenient for you, and get in touch with the study team.
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