Heart ablation after pouch closure: new registry data collected
NCT ID NCT07580937
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study gathered information from routine medical care for 198 adults with atrial fibrillation who had a prior procedure to close a small heart pouch (left atrial appendage occlusion) and later needed a heart ablation. Researchers looked at patient details, procedure steps, blood thinner use after the procedure, and any complications. The goal was to better understand how to manage these complex cases, not to test a new treatment.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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198 people
The number who actually took part.
- Started
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Mar 2022
- Finished
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Mar 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with left atrial appendage occlusion devices presenting for pulmonary vein isolation or left atrial ablation.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Individuals aged \>18 years * Undergoing any type of atrial fibrillation ablation or left atrial arrhythmia ablation Exclusion Criteria: * Missing essential baseline characteristics and/or missing collection of sufficient details regarding each complication
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Asian Heart and Vascular Center
Singapore, Singapore
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Beth Israel Deaconess Medical Center
Boston, Massachusetts, 02215, United States
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Brigham and Women's Hospital
Boston, Massachusetts, 02115, United States
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Cardioangiologisches Centrum Bethanien Frankfurt
Frankfurt, Germany
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Clinique Pasteur
Toulouse, France
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Loyola University
Chicago, Illinois, 60660, United States
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Medical University of South Carolina
Charleston, South Carolina, 29425, United States
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Nanjing Medical University
Nanjing, China
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Northwestern University
Evanston, Illinois, 60208, United States
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OLV Hospital
Aalst, Belgium
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Ospedali Riuniti Umberto I°-Lancisi-Salesi
Ancona, Italy
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Rush University Medical Center
Chicago, Illinois, 60612, United States
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University Hospital Basel
Basel, Switzerland
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University Hospital of Bern
Bern, Switzerland
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University of Chicago
Chicago, Illinois, 60637, United States
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University of Liverpool
Liverpool, United Kingdom
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University of Lübeck
Lübeck, Germany
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University of Michigan
Ann Arbor, Michigan, 48109, United States
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University of Pennsylvania
Philadelphia, Pennsylvania, 19104, United States
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Wake Forest University Health Sciences
Winston-Salem, North Carolina, 27157, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- High-resolution Contrast-Enhanced MRI of atrial fibrillation patients prior to FIRM ablation
- Assessment of flecainide to lower the patent foramen ovale closure risk of atrial arrhythmia or tachycardia
- Apple watch vs. medical monitor: which better detects hidden heart rhythm problems?
- Can a new ultrasound catheter give doctors a better view inside the heart?
- Can dropping one blood thinner cut bleeding without raising heart risks?
- Hidden heart rhythm problems after stroke: can longer monitoring prevent a second stroke?