Extended Venous Thromboembolism Prophylaxis Comparing Rivaroxaban to Aspirin Following Total Hip and Knee Arthroplasty (EPCAT II)
Primary Purpose
Venous Thromboembolism
Status
Completed
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
rivaroxaban and ASA
Sponsored by
About this trial
This is an interventional prevention trial for Venous Thromboembolism
Eligibility Criteria
Inclusion Criteria:
1. All patients undergoing elective total hip or knee arthroplasty at the participating institutions will be potentially eligible for this study
Exclusion Criteria:
- Hip or lower limb fracture in the previous three months
- 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 judgment of investigator precludes use of aspirin
- History of significant hepatic disease or any other condition that in the judgement of the investigator precludes the use of rivaroxaban
- Creatinine clearance less than 30 ml per minute
- Platelet count less than 100 x 109 /L
- Need for long-term anticoagulation due to a preexisting co-morbid condition or due to the development of venous thromboembolism following surgery but prior to randomization
- Did not or will not receive rivaroxaban post-operatively for VTE prophylaxis
- Bilateral total hip arthroplasty or simultaneous hip and knee arthroplasty
- Major surgical procedure within the previous three months
- Requirement for major surgery post arthroplasty within 90 day period
- Chronic daily aspirin use with dose greater than 100 mg a day
- Women of child bearing potential who are not abstinent or do not use appropriate contraception throughout the study drug period
- Geographical inaccessibility for follow-up
- Unwilling or unable to give consent
- Previous participation in the study
- Concomitant use with drugs that are strong inhibitors or inducers of both P-gp and CYP3A4
Sites / Locations
- Capital Health
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
rivaroxaban
ASA
Arm Description
rivaroxaban 10mg x 9 days for total knee arthroplasty patients; x 30 days for total hip athroplasty patients
ASA 81mg x 9 days for total knee arthroplasty patients; x 30 days for total hip athroplasty patients
Outcomes
Primary Outcome Measures
symptomatic venous thromboembolism
major or clinically relevant non-major bleeding
Secondary Outcome Measures
survival
myocardial infarction
stroke
wound infection
cost-effectiveness
Full Information
NCT ID
NCT01720108
First Posted
October 30, 2012
Last Updated
January 23, 2018
Sponsor
David Anderson
Collaborators
Canadian Institutes of Health Research (CIHR)
1. Study Identification
Unique Protocol Identification Number
NCT01720108
Brief Title
Extended Venous Thromboembolism Prophylaxis Comparing Rivaroxaban to Aspirin Following Total Hip and Knee Arthroplasty
Acronym
EPCAT II
Official Title
Extended Venous Thromboembolism Prophylaxis Comparing Rivaroxaban to Aspirin Following Total Hip and Knee Arthroplasty
Study Type
Interventional
2. Study Status
Record Verification Date
January 2018
Overall Recruitment Status
Completed
Study Start Date
February 24, 2013 (Actual)
Primary Completion Date
July 2016 (Actual)
Study Completion Date
July 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
David Anderson
Collaborators
Canadian Institutes of Health Research (CIHR)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
In this study the investigators want to look at whether using aspirin instead of rivaroxaban (after initial treatment with rivaroxaban) works as well at preventing blood clots while also reducing risk of bleeding and is more cost effective in patients who have either a total hip replacement or total knee replacement.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Venous Thromboembolism
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
3426 (Actual)
8. Arms, Groups, and Interventions
Arm Title
rivaroxaban
Arm Type
Active Comparator
Arm Description
rivaroxaban 10mg x 9 days for total knee arthroplasty patients; x 30 days for total hip athroplasty patients
Arm Title
ASA
Arm Type
Experimental
Arm Description
ASA 81mg x 9 days for total knee arthroplasty patients; x 30 days for total hip athroplasty patients
Intervention Type
Drug
Intervention Name(s)
rivaroxaban and ASA
Primary Outcome Measure Information:
Title
symptomatic venous thromboembolism
Time Frame
up to 4 years
Title
major or clinically relevant non-major bleeding
Time Frame
up to 4 years
Secondary Outcome Measure Information:
Title
survival
Time Frame
up to 4 years
Title
myocardial infarction
Time Frame
up to 4 years
Title
stroke
Time Frame
up to 4 years
Title
wound infection
Time Frame
up to 4 years
Title
cost-effectiveness
Time Frame
up to 4 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
1. All patients undergoing elective total hip or knee arthroplasty at the participating institutions will be potentially eligible for this study
Exclusion Criteria:
Hip or lower limb fracture in the previous three months
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 judgment of investigator precludes use of aspirin
History of significant hepatic disease or any other condition that in the judgement of the investigator precludes the use of rivaroxaban
Creatinine clearance less than 30 ml per minute
Platelet count less than 100 x 109 /L
Need for long-term anticoagulation due to a preexisting co-morbid condition or due to the development of venous thromboembolism following surgery but prior to randomization
Did not or will not receive rivaroxaban post-operatively for VTE prophylaxis
Bilateral total hip arthroplasty or simultaneous hip and knee arthroplasty
Major surgical procedure within the previous three months
Requirement for major surgery post arthroplasty within 90 day period
Chronic daily aspirin use with dose greater than 100 mg a day
Women of child bearing potential who are not abstinent or do not use appropriate contraception throughout the study drug period
Geographical inaccessibility for follow-up
Unwilling or unable to give consent
Previous participation in the study
Concomitant use with drugs that are strong inhibitors or inducers of both P-gp and CYP3A4
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David R Anderson, MD
Organizational Affiliation
Nova Scotia Health Authority
Official's Role
Principal Investigator
Facility Information:
Facility Name
Capital Health
City
Halifax
State/Province
Nova Scotia
ZIP/Postal Code
B3H 3A7
Country
Canada
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
29466159
Citation
Anderson DR, Dunbar M, Murnaghan J, Kahn SR, Gross P, Forsythe M, Pelet S, Fisher W, Belzile E, Dolan S, Crowther M, Bohm E, MacDonald SJ, Gofton W, Kim P, Zukor D, Pleasance S, Andreou P, Doucette S, Theriault C, Abianui A, Carrier M, Kovacs MJ, Rodger MA, Coyle D, Wells PS, Vendittoli PA. Aspirin or Rivaroxaban for VTE Prophylaxis after Hip or Knee Arthroplasty. N Engl J Med. 2018 Feb 22;378(8):699-707. doi: 10.1056/NEJMoa1712746.
Results Reference
derived
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Extended Venous Thromboembolism Prophylaxis Comparing Rivaroxaban to Aspirin Following Total Hip and Knee Arthroplasty
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