Atrial Fibrillation Trial, Recruiting NCT06053606 Sponsor: Wroclaw Medical University Condition: Atrial Fibrillation
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Atrial Fibrillation Trial, Recruiting

NCT06053606
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 having their first pulmonary vein isolation (PVI) procedure, which is a treatment for an irregular heart rhythm condition
  • People diagnosed with paroxysmal atrial fibrillation, meaning their irregular heart rhythm comes and goes rather than being constant
  • People whose heart is beating in a normal, regular rhythm at the time of admission
  • People whose doctor has determined they meet the medical criteria for a PVI procedure

Who may not be able to join:

  • People whose left atrial heart chamber is smaller than 38mm or larger than 50mm in size
  • People whose heart pumping function is below 40% (a measure of how well the heart is pumping blood)
  • People who have a condition where the heart's natural pacemaker does not work properly on its own
  • People with significant problems with the electrical signals that coordinate the heartbeat (confirm with trial site for specific details)
  • People who have previously had a cardioneuroablation procedure (a specific type of heart procedure targeting nerve tissue)
  • People who are pregnant
  • People for whom blood-thinning medication is not medically suitable
  • People who have any other medical reason that makes a PVI procedure unsuitable for them
  • People with a known intolerance or sensitivity to atropine (a medication sometimes used during heart procedures)

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 22 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

Principal Investigator: Piotr Niewinski, MD, PhD, Wroclaw Medical University

Phone: +48 71 733 1112

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

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Wroclaw Medical University
Registry
ClinicalTrials.gov
Start date
10 May 2024
Est. completion
31 December 2026

Where this trial is recruiting

🇵🇱 Poland

Primary endpoints

difference in the rate of persistent parasympathetic modulation

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: 22 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