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OpenTrials
Completed

NCT Number: NCT04075240

VTE Prevention Following Total Hip and Knee Arthroplasty

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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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Queen Elizabeth II HSC

Halifax, Nova Scotia, B3H 3A7, Canada

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients undergoing elective THA/TKA at the participating institutions will be potentially eligible for this study
  • Written informed consent in accordance with federal, local and institutional guidelines

Exclusion criteria

  • Previous documented VTE (proximal DVT or any PE)
  • Hip or lower limb fracture in the previous three months, not related to present surgery
  • Metastatic cancer
  • Life expectancy less than 6 months
  • History of major bleeding that in the judgment of the investigator precludes use of anticoagulant prophylaxis
  • History of aspirin allergy, active peptic ulcer disease or gastritis that in the judgment of investigator precludes use of aspirin
  • History of significant hepatic disease or any other condition that in the judgment of the investigator precludes the use of rivaroxaban
  • Creatinine clearance less than 15 ml per minute
  • Pre-operative platelet count less than 100 x 109 /L
  • Need for long-term anticoagulation due to a pre-existing co-morbid condition or due to the development of VTE following surgery but prior to randomization
  • Received anticoagulation post operatively
  • Bilateral THA/TKA or simultaneous hip and knee arthroplasty
  • Major surgical procedure within the previous 3 months
  • Requirement for major surgery post arthroplasty within a 90 day period
  • Chronic daily aspirin use with dose greater than 100 mg a day
  • Women of childbearing potential who are not abstinent or do not use effective contraception or are breast-feeding throughout the study drug period
  • Unwilling or unable to give consent
  • Previous participation in the EPCAT III study
  • Under 18 years of age
  • Concomitant use of drugs that are strong inhibitors of P-gp AND CYP3A4 (e.g., systemic treatment with ketoconazole, itraconazole, or ritonavir) or strong inducers of P-gp AND CYP3A4 (e.g., rifampicin, phenytoin, carbamazepine, phenobarbital, St. John's Wort)
  • Known allergy to food dye

Treatment and study plan

Rivaroxaban 10 MG and acetylsalicylic acid 81 mg

Drug

Starting post op, rivaroxaban (5 days) followed by aspirin (9 days for TKA; 30 days for THA)

Other names: Xarelto 10mg and aspirin 81mg

Acetylsalicylic Acid 81 mg

Drug

Starting post op, aspirin for 9 days for TKA and 30 days for THA

Other names: aspirin 81mg

Primary outcomes

  1. Venous thromboembolism

    Time frame: 90 days

    symptomatic proximal deep vein thrombosis or pulmonary embolism

  2. Bleeding

    Time frame: 90 days

    major and clinically relevant, non-major bleeds

Secondary outcomes

  1. Survival

    Time frame: 90 days

    all cause death

  2. Cost-effectiveness

    Time frame: 90 days

    quantitatively describe the costs of symptomatic thromboembolism events and major bleeding episodes

Sponsors and collaborators

Lead sponsor

Sudeep Shivakumar

Other

Collaborators

  • Canadian Institutes of Health Research (CIHR)
  • Canadian Venous Thromboembolism Clinical Trials and Outcomes Research (CanVECTOR) Network
  • Nova Scotia Health Authority

Registry information

Official study title

Extended Venous Thromboembolism Prophylaxis Comparing Rivaroxaban and Aspirin to Aspirin Alone Following Total Hip and Knee Arthroplasty (EPCATIII)

Acronym: EPCATIII

Important dates

Study start
2021
Primary completion
2025
Study completion
2026
First posted
Aug 30, 2019
Registry last updated
Jun 16, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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