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NCT number NCT02889562
Study type Interventional
Source Sanford Health
Contact Lora Black
Phone 6053126436
Status Recruiting
Phase Phase 2/Phase 3
Start date September 2016
Completion date December 2018

Clinical Trial Summary

In this open-label, prospective, randomized pilot study, patients who develop atrial fibrillation after isolated coronary artery bypass grafting surgery will be identified. Patients with persistent atrial fibrillation (>12 hours) or recurrent sustained atrial fibrillation (>2 episodes of atrial fibrillation lasting longer than 30 minutes) will be candidates for inclusion. Upon meeting study inclusion and exclusion criteria, and after informed consent, patients will be randomized to either the standard of care (warfarin per protocol) or apixaban arms of the trial. Routine postoperative care after CABG will occur in both groups. Upon discharge, anticoagulation in both groups will be managed by the anticoagulation clinic. Patients will be followed for 30 days after surgery.

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

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