Clinical Trial: Vascular Closure With a Device Compared to Manual Compression After Atrial Fibrillation Ablation: The LockeT II Study
Study Status: Completed
Recruit Status: RECRUITING
Condition: Atrial Fibrillation
Study Type: INTERVENTIONAL
Official Title: Vascular Closure With Novel Ergonomic External Compression Device Compared to Manual Compression After Atrial Fibrillation Ablation: The LockeT II Study
Brief Summary:
The LockeT II study is a single center, prospective randomized study.It is intended to study the effectiveness of using LockeT device to gain hemostasis after venous procedures as compared to Manual Compression (MC).Approximately 110 patients will be enrolled.
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