NCT05014802 Baseline Atrial Fibrosis Predicts Risk for Post-operative Atrial Fibrillation in Patients Undergoing Cardiac Surgery
| NCT ID | NCT05014802 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Tulane University |
| Condition | Atrial Fibrillation |
| Study Type | OBSERVATIONAL |
| Enrollment | 50 participants |
| Start Date | 2021-11-21 |
| Primary Completion | 2026-08 |
Trial Parameters
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
Brief Summary
The study aims to evaluate and compare the incidence of atrial arrhythmias (including Post-Operative Atrial Fibrillation (POAF), atrial flutter, and atrial tachycardia) stratified by baseline Utah fibrosis stages and overall fibrosis (%) of the left atrial wall area. The investigators hypothesize that patients with a higher baseline Utah fibrosis staging will experience a higher incidence of POAF. The study also aims to evaluate and compare the in-hospital mortality, length-of-stay (LOS), complication rates (strokes, pneumonia, respiratory failure etc.) of the different Utah fibrosis stage cohorts. Perform cost analysis and compare between patients with POAF and patients without POAF. The investigators hypothesize that patients experiencing POAF will have a higher mortality rate, longer LOS, greater complications, and therefore, additional hospital costs.
Eligibility Criteria
Inclusion Criteria: * Male or female patients age 40 years of age or older * Patients with no history of atrial arrhythmia (atrial fibrillation, atrial flutter, atrial tachycardia) scheduled to undergo cardiac surgery (These surgeries include but are not limited to coronary artery bypass graft (CABG), valvular repair/reconstruction, aneurysm repair, and insertion of pacemaker). Exclusion Criteria: * Patients with a history of atrial arrhythmia (atrial fibrillation, atrial flutter, atrial tachycardia) * Patients with a history of cardiac or open chest surgery * Patients with a history of catheter ablation * Patients under the age of 40 * Patients with left ventricular assist device (LVAD) or scheduled to have LVAD implanted * Patients who have previously undergone extracorporeal membrane oxygenation (ECMO) * Patients who have undergone or will undergo heart transplantation * Patients with any health related Late Gadolinium Enhancement (LGE)-MRI contraindications (including previous alle
Related Trials
Related Intelligence Guides
In-depth guides covering this condition's trials, eligibility, and what to expect.