Clinical Trial: MIFI Flutter Registry - Ablation of Atrial Flutter With IntellaTip Sensor Technology

Study Status: Not yet recruiting
Recruit Status: Not yet recruiting
Study Type: Observational [Patient Registry]

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Official Title: Prospective Atrial Flutter Ablation Registry Investigating IntellaTip Mifi XP 8 mm Technology and Maximum Voltage-guided (MVG) Isthmus Ablation Approach

Brief Summary:

• Prospective Atrial Flutter Ablation Registry investigating IntellaTip Mifi XP 8 mm technology and MVG isthmus ablation approach
• Design: National, multi-centre, prospective observational registry documenting right atrial isthmus ablation
• Observational treatment: Combination of MVG ablation strategy and the IntellaTip Mifi XP 8 mm sensor technology
• Duration: Patients will be followed for 6 months post-ablation