New breathing trick may steady catheters during heart ablation
NCT ID NCT07402798
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a special breathing technique during atrial fibrillation ablation to see if it reduces catheter movement. Fifty-two adults with atrial fibrillation were given both standard and high-frequency, low-volume ventilation during their procedure. The goal was to see if the new method keeps the catheter more stable, which could make the ablation more precise and safer.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this breathing technique could make heart ablation procedures more stable and potentially safer, improving outcomes for atrial fibrillation patients.
- What could go wrong
- This is a small pilot study with only 52 participants. The findings are preliminary and need confirmation in larger trials. The special breathing method may not work for all patients or could cause side effects.
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
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52 people
The number who actually took part.
- Started
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May 2025
- Finished
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Feb 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
Adult patients with paroxysmal, persistent, or permanent atrial fibrillation (AF) scheduled for radiofrequency ablation (RFA) under general anesthesia.
- Ages
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21 to 85 years
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults aged 21-85 years. * Diagnosed with paroxysmal, persistent, or permanent atrial fibrillation (AF). * Scheduled for radiofrequency ablation (RFA) under general anesthesia. * Patients undergoing repeat ablation procedures included for evaluation of ventilatory, anesthetic, and post-anesthesia recovery parameters. * Patients undergoing repeat ablation procedures excluded from analyses related to procedural efficacy outcomes. Exclusion Criteria: * Left or right ventricular dysfunction. * Severe tricuspid regurgitation. * Severe pulmonary hypertension. * Severe chronic obstructive pulmonary disease (COPD) with evidence of auto-positive end-expiratory pressure. * Uncontrolled severe asthma. * Chronic metabolic acidosis with associated hyperkalemia. * Severe migraine disorders. * Trigeminal neuralgia. * Atypical facial pain. * Advanced hydrocephalus. * Presence of ventriculoperitoneal shunt. * Parkinson's disease. * Epilepsy. * Vertigo. * Ménière's disease. * Narrow-angle glaucoma. * Prior stroke with persistent neurological deficits.
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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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Teknon Medical Center
Barcelona, Barcelona, Spain, 08022, Spain
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