TactiCath Post Market Approval Study | Clinical Research Studies Listing

Recruiting

18 years - 100 years

All

Phase 4

35 participants needed

1 Location

Brief description of study

The purpose of the research study is to obtain additional information safety and effectiveness of an FDA approved catheter when used to treat patients with Paroxysmal atrial fibrillation.

Detailed description of study

The purpose of the study is to provide data and safety for the Food and Drug administration (FDA). The study is designed for patients with paroxysmal atrial fibrillation. Participants will only be enrolled if at the time of consent present with paroxysmal atrial fibrillation and meet criteria for an ablation procedure. The study is seeking participants willing to be followed for a period of 5 years

Eligibility of study

You may be eligible for this study if you meet the following criteria:

Conditions: Atrial Fibrillation
Age: 18 years - 100 years
Gender: All

Updated on 19 Feb 2024. Study ID: 821652

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