Registry collecting imaging data for patients with atrial fibrillation

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational registry aims to gather a curated dataset of multimodal imaging data from patients with atrial fibrillation or flutter who undergo transesophageal echocardiography prior to catheter ablation or cardioversion. The study focuses on utilizing artificial intelligence to analyze transthoracic echocardiography video images combined with clinical data to predict the presence of left atrial appendage thrombus. By developing and validating an AI model, the study seeks to enhance risk prediction and outcomes for these patients.

Why it matters

Who can join: the full rules

Inclusion Criteria:

\- All patients with AF or AFl in whom TEE will be performed (to assess their eligibility for cardioversion or ablation), hospitalized in a participating center during study period (all consecutive patients).

Exclusion Criteria:

Age\<18, lack of informed, written consent to the TEE

Where it's running

• Nowa Sol Multidyscyplinary Hospital
  Nowa Sól, Lubusz Voivodeship, Poland Recruiting
• John Paul II Hospital
  Krakow, Poland Recruiting
• Military Institute of Medicine National Research Institute
  Warsaw, Poland Recruiting
• Collegium Medicum, University of Zielona Góra
  Zielona Góra, Poland Recruiting
• St. Anne Hospital
  Brno, Czechia Not yet recruiting
• Medical University of Silesia
  Katowice, Poland Not yet recruiting

Study contacts

• Principal investigator: Konrad Pieszko, MD, PhD — University of Zielona Gora
• Study coordinator: Konrad Pieszko, MD, PhD
• Email: k.pieszko@cm.uz.zgora.pl
• Phone: +48728358082

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Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.