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NCT06526546Completed

ADVENT Trial Long Term Outcomes Evaluating Atrial Fibrillation Progression Study

ADVENT Trial Long Term Outcomes Evaluating Atrial Fibrillation Progression (ADVENT LTO Study)

Source: ClinicalTrials.gov · Last updated 2 Mar 2026

Brief summary (registry, in English)

The (ADVENT LTO) is an observational, non-significant risk study to assess the progression of atrial fibrillation in subjects who received ablation treatment with either the FARAPULSE Pulsed Field Ablation System or thermal ablation in the ADVENT Trial.

Status (registry)
Completed
Study type
Observational
Enrollment
364 (actual)
First submitted
25 Jul 2024
Start date
31 Oct 2024
Primary completion date
8 Dec 2025
Lead sponsor
Boston Scientific Corporation
NCT number
NCT06526546

What you commit to

  • Study type: Observational
  • Participants enrolled: 364
  • From 31 Oct 2024 to the primary completion date, 8 Dec 2025
  • 25 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • There are no exclusion criteria for this study.

Who the study is looking for

  • Subjects who meet all of the following criteria may be given consideration for inclusion in this clinical investigation.
  • Subjects who were enrolled, randomized and treated for paroxysmal atrial fibrillation, classified as Modified Intention-to-Treat subjects, and completed the 12-Month Follow-Up in the FARAPULSE ADVENT Trial (CIP CS0934; NCT04612244).
  • Subjects or legally authorized representatives who are willing and capable of providing informed consent.
  • Subjects who are willing to comply with the protocol requirements.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (25)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Emory University Hospital
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AtlantaUnited StatesUnknown status
Texas Cardiac Arrhythmia Research
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AustinUnited StatesUnknown status
Johns Hopkins Hospital
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BaltimoreUnited StatesUnknown status
Grandview Medical Center
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BirminghamUnited StatesUnknown status
St. Lukes Idaho Cardiology Associates
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BoiseUnited StatesUnknown status
Beth Israel Deaconess Medical Center
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BostonUnited StatesUnknown status
Massachusetts General Hospital (MGH)
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BostonUnited StatesUnknown status
Mills Peninsula Health Services
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BurlingameUnited StatesUnknown status
Trident Medical Center
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CharlestonUnited StatesUnknown status
Medical University of South Carolina
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CharlestonUnited StatesUnknown status
Doylestown Hospital
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DoylestownUnited StatesUnknown status
St. Luke's Hospital of Kansas City
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Kansas CityUnited StatesUnknown status
Scripps Memorial Hospital
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La JollaUnited StatesUnknown status
Vanderbilt University Medical Center
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NashvilleUnited StatesUnknown status
St. Thomas Research Institute, LLC
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NashvilleUnited StatesUnknown status
Northwell Health
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New YorkUnited StatesUnknown status
Mount Sinai - Icahn School of Medicine
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New YorkUnited StatesUnknown status
Nebraska Methodist Hospital
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OmahaUnited StatesUnknown status
Presbyterian University of Pennsylvania Medical Center
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PhiladelphiaUnited StatesUnknown status
Banner-University Medical Center Phoenix
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PhoenixUnited StatesUnknown status
Providence St. Vincent Medical Center
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PortlandUnited StatesUnknown status
Virginia Commonwealth University Health System
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RichmondUnited StatesUnknown status
University of California San Francisco
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San FranciscoUnited StatesUnknown status
Washington Hospital Center
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Washington D.C.United StatesUnknown status
Pinnacle Health at Harrisburg Hospital
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WormleysburgUnited StatesUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.