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New breathing trick may steady catheters during heart ablation

NCT ID NCT07402798

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

52 people

The number who actually took part.

Started

May 2025

Finished

Feb 2026

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

Adult patients with paroxysmal, persistent, or permanent atrial fibrillation (AF) scheduled for radiofrequency ablation (RFA) under general anesthesia.

Ages

21 to 85 years

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

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

  • Teknon Medical Center

    Barcelona, Barcelona, Spain, 08022, Spain

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