Multimodal, Multicentre Registry of Clinical and Imaging Data to Develop Predictive Models Based on Artificial Intelligence to Support the Diagnostic and Therapeutic Process for Patients with Atrial Fibrillation Undergoing Catheter Ablation and Cardioversion.

Status: Recruiting
Location: See all (6) locations...
Intervention Type: Procedure, Diagnostic test
Study Type: Observational
SUMMARY

The goal of this observational registry is to collect a curated dataset of multimodal imaging data that will serve for development of artificial-intelligence based solutions for prediction of risk and outcomes in patients with atrial fribrillation. Type of study: observational study Study Participants: Patients with atrial fibrillation or atrial flutter who undergo clinically indicated transesophageal echocardiography before catheter ablation or cardioversion. We hypothesize, that automatic analysis of video images of transthoracic echocardiography with deep learning combined with clinical data can predict the presence of left atrial appendage thrombus (LAT). Therefore, our main aim is to create and validate an artificial intelligence model to predict the presence of LAT based on automatic analysis of transthoracic echocardiography with artificial intelligence.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• \- 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).

Locations
Other Locations
Poland
Medical University of Silesia
NOT_YET_RECRUITING
Katowice
John Paul II Hospital
RECRUITING
Krakow
Nowa Sol Multidyscyplinary Hospital
RECRUITING
Nowa Sól
Military Institute of Medicine National Research Institute
RECRUITING
Warsaw
National Institute of Cardiology
NOT_YET_RECRUITING
Warsaw
Collegium Medicum, University of Zielona Góra
RECRUITING
Zielona Góra
Contact Information
Primary
Konrad Pieszko, MD, PhD
k.pieszko@cm.uz.zgora.pl
+48728358082
Time Frame
Start Date: 2024-01-01
Estimated Completion Date: 2027-09
Participants
Target number of participants: 3000
Treatments
AF or AFl patients
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.
Sponsors
Collaborators: Military Institute od Medicine National Research Institute, Nowa Sol Multidyscyplinary Hospital, Poland, John Paul II Hospital, Krakow, National Institute of Cardiology, Warsaw, Poland, St. Anne's University Hospital Brno, Czech Republic, Medical University of Silesia, Katowice, Poland
Leads: University in Zielona Góra

This content was sourced from clinicaltrials.gov