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RECRUITING
NCT04642430
PHASE4

COmparison of Bleeding Risk Between Rivaroxaban and Apixaban in Patients With Atrial Fibrillation

Sponsor: Ottawa Hospital Research Institute

View on ClinicalTrials.gov

Summary

Atrial Fibrillation (AF) affects 200,000 Canadians and increases risk of stroke, morbidity and mortality. Having a stroke can affect a patient's ability to speak, eat, walk, work, care for themselves, and interact with others. Not only can it ruin one's life, but it can also be fatal. A stroke occurs when blood flow to the brain is blocked by a clot, depriving brain cells of oxygen. In people with atrial fibrillation, blood flow is sluggish in the top chambers of the heart, and blood clots can form there. When a piece of a clot breaks off, it can travel to the brain and cause a stroke. That's where blood thinners come in. Blood thinners, or anticoagulants, decrease the chances of blood clots forming in the heart, reducing the risk of stroke. Studies show that blood thinners are highly effective at reducing the risk of stroke by up to 95%. The conventional blood thinner is warfarin, taken by mouth. Warfarin requires regular blood tests to make sure a patient getting the correct dose. The patient also may have to avoid certain foods since the medication can interact with them. Newer blood thinners, known as direct-oral anticoagulants (DOACs) are available, which do not require regular blood tests and do not interact with foods. Two of the new blood thinners are called rivaroxaban and apixaban. Like warfarin, they can be taken by mouth, and studies have shown them to be as effective as warfarin. Both rivaroxaban and apixaban have been approved for stroke prevention in AF by Health Canada. However, there have been no direct head-to-head comparisons of these two anticoagulants, meaning comparative safety data is not available. Increasing use of DOACs for stroke prevention in AF and patient values around bleeding highlight the need for a comparison trial to ensure patients receive the anticoagulant with the greatest balance of benefit to potential harm. The trial is to assess bleeding rates and superiority of using apixaban versus rivaroxaban in patients with non-valvular atrial fibrillation.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

3018

Start Date

2021-07-06

Completion Date

2027-12-31

Last Updated

2025-11-17

Healthy Volunteers

No

Interventions

DRUG

Apixaban

Refer to Apixaban group

DRUG

Rivaroxaban

Refer to Rivaroxaban group

Locations (8)

Victoria Cardiac Arrhythmia Trials

Victoria, British Columbia, Canada

QEII Health Science Centre

Halifax, Nova Scotia, Canada

Kingston General Hospital

Kingston, Ontario, Canada

The Ottawa Hospital - General Campus

Ottawa, Ontario, Canada

University Ottawa Heart Institute

Ottawa, Ontario, Canada

CISSS de l'Outaouais

Gatineau, Quebec, Canada

CHU de Quebec - Université Laval

Laval, Quebec, Canada

Ciusss Nim

Montreal, Quebec, Canada