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Clinical Trial Summary

This prospective, randomized, controlled, unblinded, multicenter study aims at comparing procedural time between conventional CLOSE-guided pulmonary vein isolation (PVI) (35W/50W) versus very high power radiofrequency delivery (90W) in atrial fibrillation patients scheduled for a first PVI.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04784013
Study type Interventional
Source AZ Sint-Jan AV
Contact
Status Completed
Phase Phase 4
Start date March 24, 2021
Completion date May 31, 2022

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