EICHORCondition: Atrial Arrhythmia · Atrial Fibrillation · Paroxysmal Atrial Fibrillation · Sponsor: Abbott Medical Devices
This clinical investigation is intended to demonstrate safety and effectiveness of the Volt™ Pulsed Field Ablation (PFA) Catheter Sensor Enabled™, the Volt™ PFA Generator, Agilis™ NxT Steerable Introducer Dual-Reach™, and EnSite™ X EP System EnSite™ Pulsed Field Ablation Module (for simplicity of reference this device collection will hereafter be referred to as the Volt™ PFA system) for the treatment of symptomatic, recurrent, drug-refractory paroxysmal and persistent atrial fibrillation.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
| Affinity Cardiovascular Specialists, LLC | Birmingham, Alabama, United States | — |
| Arkansas Heart Hospital | Little Rock, Arkansas, United States | — |
| Cedars-Sinai Medical Center | Los Angeles, California, United States | — |
| California Pacific Medical Center - Van Ness Campus | San Francisco, California, United States | — |
| South Denver Cardiology Associates PC | Littleton, Colorado, United States | — |
| Medical Center of the Rockies | Loveland, Colorado, United States | — |
| Washington Hospital Center | Washington D.C., District of Columbia, United States | — |
| AdventHealth Orlando | Orlando, Florida, United States | — |
| AdventHealth Tampa | Tampa, Florida, United States | — |
| Emory University Hospital | Atlanta, Georgia, United States | — |
| Northside Hospital | Atlanta, Georgia, United States | — |
| Northwestern Memorial Hospital | Chicago, Illinois, United States | — |
+ 28 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT06223789