This study is a registry study. The purpose is to collect information over time about how Medtronic products are working and/or the outcome of the treatment. The registry will be used to support post-market surveillance activities and post-approval studies (e.g., to collect safety and performance information). In addition, it will be used to obtain clinical evidence for the development and improvement of medical devices, therapies, device guidelines, patient services/solutions and provide clinical data to support health economics and clinical outcomes research. The registry is not an experimental clinical study.
Contact phoneSparrow Clinical Research Institute | 517.364.5760
Principal investigatorDr. John Ip, MD, FACC
Trial CategoryHeart & Vascular
Trial SubCategoryCardiac Arrhythmia