NCT06584266Recruiting
Multimodal Cardiac Imaging Registry in Patients with Atrial Fibrillation
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.
Source: ClinicalTrials.gov · Last updated 4 Sept 2024 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 3000 (estimated)
- First submitted
- 31 Aug 2024
- Start date
- 1 Jan 2024
- Primary completion date
- Sept 2026
- Lead sponsor
- University in Zielona Góra
- Diseases
- Heart failure, Atrial fibrillation
- NCT number
- NCT06584266
What you commit to
- Study type: Observational
- Planned participants: 3000
- From 1 Jan 2024 to the primary completion date, Sept 2026
- 7 sites in 2 countries
- 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.
Age
- Age\<18, lack of informed, written consent to the TEE
Who the study is looking for
- \- 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).
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (7)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| St. Anne Hospital Coordinator of this site? Confirm its status | Brno | Czechia | Not yet recruiting |
| Medical University of Silesia Coordinator of this site? Confirm its status | Katowice | Poland | Not yet recruiting |
| John Paul II Hospital Coordinator of this site? Confirm its status | Krakow | Poland | Recruiting |
| Nowa Sol Multidyscyplinary Hospital Coordinator of this site? Confirm its status | Nowa Sól | Poland | Recruiting |
| National Institute of Cardiology Coordinator of this site? Confirm its status | Warsaw | Poland | Not yet recruiting |
| Military Institute of Medicine - National Research Institute Coordinator of this site? Confirm its status | Warsaw | Poland | Recruiting |
| Collegium Medicum, University of Zielona Góra Coordinator of this site? Confirm its status | Zielona Góra | Poland | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.