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Coronary Computed Tomography AngioGraphy Prior to Catheter Ablation in Patients With Atrial FIBrillation

Study acronym: FIBCAG
StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Minor Eligibility criteria expanded, about 6 wordsv5
  2. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Mar 15, 2024 to Mar 26, 2024
    • Study description revised
    • Site details revised
    v4
  3. Notable Start date: Oct 1, 2023 to Mar 15, 2024
    • Interventions: Analysis of coronary CT Angiography and CAC scoring prior to catheter ablation (Diagnostic Test) to Analysis of coronary CT Angiography and CAC scoring at the time of catheter ablation (Diagnostic Test)
    • Secondary endpoints: 8 to 10
    • Study description expanded, about 227 words
    v3
  4. Notable Primary endpoint revised
    • Secondary endpoints: 7 to 8
    • Study description expanded, about 9 words
    v2
  5. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT05978388
Lead Sponsor Tor Biering-Sørensen
Conditions
(from sponsor)
Atrial Fibrillation
Related terms Atherosclerosis, Atrial Fibrillation, Cardiovascular Diseases, Coronary Artery Disease, Myocardial Ischemia
Enrollment 852 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov