IMPROVED-AF STUDY
Brief description of study
This is a post-market, prospective, multi-center, two-arm randomized-controlled clinical study. Subjects will be randomized in a 1:1 ratio into two arms: a treatment arm (use of vMap system in addition to pulmonary vein isolation [vMap+PVI]) and a control arm (PVI alone).The study is designed to compare clinical outcomes following use of an FDA-cleared vMap for mapping for subjects w/ AF.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Medical Research
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Age: 99 years or below
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Gender: All
TBD
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