CONVERGE
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- STATUS
- Recruiting
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- sponsor
- AtriCure
Summary
CONVERGE
Description
This study is evaluating 2 different treatment options for persistent atrial fibrillation. In this multi-center, pivotal clinical study, patients are randomized (2:1) to either a convergent procedure that includes both epicardial and endocardial atrial ablation versus standalone endocardial catheter ablation. The study will enroll and randomize one hundred and fifty three (153) patients from up to thirty (30) sites with twenty-seven (27) in the US and three (3) sites OUS.
Study participants will need to come for procedure follow-up visits at 7 days, 1 month, 3 months, 6 months and 12 months after undergoing the study procedure.
Study participants will be continued to be followed long term with an office visit at 18months and phone follow-up after that at year 2, 3, 4, and 5 post procedure.
Details
| Condition | Atrial Fibrillation, Atrial Flutter, Fast Heart Rate (Tachycardia) |
|---|---|
| Clinical Study Identifier | TX145279 |
| Sponsor | AtriCure |
| Last Modified on | 23 November 2020 |
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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