Actively Recruiting
Coronary Computed Tomography AngioGraphy Prior to Catheter Ablation in Patients With Atrial FIBrillation
Led by Tor Biering-Sørensen · Updated on 2024-06-26
852
Participants Needed
1
Research Sites
209 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this randomized, controlled trial is to investigate whether coronary computed tomography (CT) angiography prior to catheter ablation and derived treatment (medical anti-ischemic and multimodality treatment and/or mechanical revascularization) can improve clinical outcomes in patients with atrial fibrillation undergoing catheter ablation. A sub-study will investigate the effect of different ablation strategies on clinical outcomes in patients with atrial fibrillation undergoing catheter ablation.
CONDITIONS
Official Title
Coronary Computed Tomography AngioGraphy Prior to Catheter Ablation in Patients With Atrial FIBrillation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 18 years
- Referral for catheter ablation treatment (excluding AV-junction ablation) for atrial fibrillation, including both paroxysmal and persistent types
- Includes patients undergoing first ablation or re-ablation
- Ability and willingness to provide written informed consent
You will not qualify if you...
- Known atherosclerotic cardiovascular disease
- Currently treated with statins
- Contraindication for coronary CT angiography, such as contrast allergy
- Recent coronary CT angiography including CAC scoring without positive findings within 3 years prior to screening
- Any medical or surgical condition that increases risk or may prevent study completion, as judged by the investigator
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Center for Translational Cardiology and Pragmatic Randomized Trials, Department of Cardiology, Copenhagen University Hospital - Herlev and Gentofte
Hellerup, Capital Region, Denmark, 2900
Actively Recruiting
Research Team
C
Caroline Espersen, MD
CONTACT
T
Tor Biering-Sørensen, MD, PhD, MPH, MSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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