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Apixaban for the Reduction of Thromboembolism in Patients With Device-Detected Subclinical Atrial Fibrillation
THE PURPOSE OF THIS CLINICAL TRIAL IS TO DETERMINE WHICH TREATMENT IS BEST FOR PREVENTING STROKE OR SYSTEMIC EMBOLISM IN PATIENTS WHO HAVE EXPERIENCED AT LEAST ONE DEVICE-DETECTED EPISODE OF ATRIAL FIBRILLATION AND WHO ALSO HAVE OTHER RISK FACTORS FOR STROKE. THIS IS A SUMMARY OF THE CLINICAL TRIAL. ONCE YOU CONTACT US, WE WILL PROVIDE YOU WITH ALL THE INFORMATION YOU NEED.
Technical Summary
- APIXABAN FOR THE REDUCTION OF THROMBOEMBOLISM IN PATIENTS WITH DEVICE-DETECTED SUBCLINICAL ATRIAL FIBRILLATION
- Code EudraCT: 2014-001397-33
- Protocol number: ARTESIA
- Promoter: Population Health Research Institute (PHRI)
- Molecule/Drug: Apixabán
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* The trials only admit a limited number of patients and are subject to inclusion and exclusion criteria. The specialist who assesses your case will inform you of the conditions required to participate in the clinical trial.
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