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NCT07809347Recruiting

Evaluation of the Factors Associated With BRADYcardia Following Pulmonary Vein Isolation Using Pulsed Field Ablation

Evaluation of the Factors Associated With Bradtycardia Following Pulmonary Vein Isolation Using Pulsed Field Ablation

Source: ClinicalTrials.gov · Last updated 9 Sept 2026

Brief summary (registry, in English)

The study aims to identify factors associated with bradycardia during the hospital stay after ablation of atrial fibrillation performed with pulsed field technology.

Status (registry)
Recruiting
Study type
Observational
Enrollment
100 (estimated)
First submitted
29 Aug 2026
Start date
1 Jan 2026
Primary completion date
31 Dec 2026
Lead sponsor
Wroclaw Medical University
NCT number
NCT07809347

What you commit to

  • Study type: Observational
  • Planned participants: 100
  • From 1 Jan 2026 to the primary completion date, 31 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Cardiac tamponade
  • Acute stroke
  • Acute bleeding requiring surgical intervention

Other

  • Permanent pacemaker
  • CRT device
  • Dual-chamber ICD

Who the study is looking for

  • \- Pulmonary vein isolation performed with PFA

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Institute of Heart Diseases, Wroclaw Medical University
Coordinator of this site? Confirm its status
WroclawPolandRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.