Heart ablation may change stroke risk – new study investigates
NCT ID NCT05635864
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study followed 167 people with atrial fibrillation or flutter who had a catheter ablation procedure. Researchers measured changes in stroke and bleeding risk scores before and 3, 6, and 12 months after ablation. They also compared different monitoring methods, including implantable devices and smartwatches, to detect any return of abnormal heart rhythms.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- catheter ablation
- What this could lead to
- If successful, this could help doctors better predict stroke and bleeding risks after ablation, improving personalized care for atrial fibrillation patients.
- What could go wrong
- This is a small, non-randomized study that only measures risk scores, not actual stroke or bleeding events. Results may not apply to all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
167 people
The number who actually took part.
- Started
-
Jun 2021
- Finished
-
Nov 2025
- Lead sponsor
-
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 planned to undergo first catheter ablation for symptomatic atrial tachyarrhythmias (atrial fibrillation, atrial flutter) will be enrolled.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
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: * Symptomatic atrial tachyarrhythmias (atrial fibrillation, atrial flutter) * Planned for 1st right or left atrial ablation * Informed consent * at least 18 years Exclusion Criteria: * Previous left or right atrial ablation * Ineligibility for catheter ablation * History of TIA / stroke * \< 18 years * LA thrombus formation or history of thrombus formation
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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
-
Hannover Medical School
Hanover, Lower Saxony, 30625, Germany
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Heart hole or stroke trigger? global registry tracks who gets closure and what happens next
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