Atrial Fibrillation Trial, Recruiting NCT06207383 Sponsor: University Hospital, Geneva Condition: Atrial Fibrillation
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Atrial Fibrillation Trial, Recruiting

NCT06207383
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have persistent atrial fibrillation (an irregular heart rhythm that does not stop on its own) along with heart failure symptoms that have not improved enough with medication, and who have been assessed as suitable for a heart procedure called AF ablation, with no more than one previous procedure to isolate the pulmonary veins in the heart.
  • People who have been admitted to hospital, or visited an emergency room or heart failure clinic at least once in the past 2 years because of heart failure, and who had a specific blood marker (NT-pro-BNP above 1000 pg/ml or BNP above 250 pg/ml) measured at some point during that period.
  • People who have previously taken, or are currently taking, medication to control their heart rate or heart rhythm.
  • People who are older than 60 years of age.

Who may not be able to join:

  • People with very severe heart failure symptoms (classified as NYHA Class IV) and a very low blood pressure (at or below 80 mmHg) even after receiving the best available treatment.
  • People whose life expectancy is less than 2 years.
  • People who need a major surgical procedure.
  • People who have had a heart attack, stroke, or a heart procedure called PCI within the past 3 months.
  • People who already have, or are planned to receive, a device that helps the heart beat in a coordinated way (called a CRT device) or a pacemaker. A device used only to prevent dangerous heart rhythms (an ICD), without a need for pacing, is acceptable.
  • People who are currently participating in another controlled clinical trial.
  • People who are not able to sign an informed consent form.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: +41794616217

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
University Hospital, Geneva
Registry
ClinicalTrials.gov
Start date
1 October 2024
Est. completion
1 June 2028

Where this trial is recruiting

🇦🇹 Austria 🇧🇪 Belgium 🇧🇬 Bulgaria 🇨🇿 Czechia 🇫🇮 Finland 🇫🇷 France 🇩🇪 Germany 🇭🇺 Hungary 🇮🇹 Italy 🇳🇱 Netherlands 🇵🇱 Poland 🇪🇸 Spain 🇨🇭 Switzerland 🇬🇧 United Kingdom

Primary endpoints

Superiority endpoint; Non-inferiority endpoint

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov