nMARQ Pulmonary Vein Isolation System for the Treatment of Paroxysmal Atrial Fibrillation

  • STATUS
    Recruiting
  • participants needed
    1
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Updated on 19 February 2024

Summary

Subjects with symptomatic PAF who have had at least one AF episode documented within one (1) year prior to enrollment and who have failed at least one antiarrhythmic drug (AAD). The Main Study will consist of a prospective, multi-center, randomized (1:1 concurrent nMARQ Catheter System [nMARQ] vs THERMOCOOL® Navigational Family of catheters [TC]), controlled, two-arm, single-blind design. Embedded within the Main Study will be a Subpopulation Neurological Assessment (SNA) with a prospective, controlled design, with consecutive enrollment.

Details
Condition Atrial Fibrillation, atrial fibrillation
Age 1years - 99years
Clinical Study Identifier817909
Last Modified on19 February 2024

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