Queen Elizabeth II HSC
Halifax, Nova Scotia, B3H 3A7, Canada
NCT Number: NCT04075240
Consented patients undergoing elective total hip and total knee arthroplasty will be randomized to receive either aspirin alone or aspirin and rivaroxaban for prevention of venous thromboembolism.
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Notify Me18 year and older
All sexes
Interventional
Phase 3
Halifax, Nova Scotia, B3H 3A7, Canada
Aspirin and rivaroxaban prevent venous thromboembolism (VTE) via different mechanisms. Aspirin is significantly cheaper than rivaroxaban. Aspirin in combination with rivaroxaban was shown to be safe and efficacious in a non-inferiority trial (EPCATII) when compared to rivaroxaban alone.
This study will assess if aspirin alone is non-inferior to rivaroxaban and aspirin in the prevention of venous thromboembolism.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Starting post op, rivaroxaban (5 days) followed by aspirin (9 days for TKA; 30 days for THA)
Other names: Xarelto 10mg and aspirin 81mg
Starting post op, aspirin for 9 days for TKA and 30 days for THA
Other names: aspirin 81mg
Time frame: 90 days
symptomatic proximal deep vein thrombosis or pulmonary embolism
Time frame: 90 days
major and clinically relevant, non-major bleeds
Time frame: 90 days
all cause death
Time frame: 90 days
quantitatively describe the costs of symptomatic thromboembolism events and major bleeding episodes
Sudeep Shivakumar
Other
Extended Venous Thromboembolism Prophylaxis Comparing Rivaroxaban and Aspirin to Aspirin Alone Following Total Hip and Knee Arthroplasty (EPCATIII)
Acronym: EPCATIII
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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