Xarelto for Thromboprophylaxis After Total Hip and Total Knee Arthroplasty
Primary Purpose
Venous Thromboembolism, Arthroplasty
Status
Recruiting
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Rivaroxaban 10 MG
Sponsored by
About this trial
This is an interventional prevention trial for Venous Thromboembolism
Eligibility Criteria
Inclusion Criteria:
- Undergo total knee replacement or total hip replacement
Exclusion Criteria:
- Recent antithrombotics use
- A history of a coagulopathy
- Recent thromboembolic disease
- Preoperative deep vein thrombosis screening presents positive
- Age below 20
Sites / Locations
- Ditmanson Medical Foundation Chiayi Christian HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Rivaroxaban
Control
Arm Description
The participants are provided with Rivaroxaban 10mg
The participants are provided without antithrombotics
Outcomes
Primary Outcome Measures
Deep vein thrombosis
The incidence of both asymptomatic and symptomatic deep vein thrombosis
Pulmonary embolism
The incidence of pulmonary embolism
Secondary Outcome Measures
Complication
Major bleeding, infection, and non-healing wound
Full Information
NCT ID
NCT05449327
First Posted
June 29, 2022
Last Updated
October 2, 2023
Sponsor
Chiayi Christian Hospital
1. Study Identification
Unique Protocol Identification Number
NCT05449327
Brief Title
Xarelto for Thromboprophylaxis After Total Hip and Total Knee Arthroplasty
Official Title
Xarelto for Thromboprophylaxis After Total Hip and Total Knee Arthroplasty
Study Type
Interventional
2. Study Status
Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 1, 2023 (Actual)
Primary Completion Date
December 21, 2025 (Anticipated)
Study Completion Date
December 21, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Chiayi Christian Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
5. Study Description
Brief Summary
Venous thromboembolism is a serious complication after total hip replacement (THR) and total knee replacement (TKR). Previous studies have reported the incidence of both asymptomatic and symptomatic deep vein thrombosis (DVT) after TKR were higher in Taiwan than other countries in Asia. Therefore, the usage of prophylactic antithrombotics should be considered. The efficacy and safety of Xarelto (Rivaroxaban) for preventing venous thromboembolism has been proved. However, there is a lack of study using prospective design to evaluate the efficacy and safety of Xarelto after THR and TKR for Taiwanese. In this study, the investigators use a randomized controlled trial design comparing the incidence of DVT, pulmonary embolism, and complications between intervention and control groups.
Detailed Description
This parallel study is conducted in a single hospital. The participants are divided into two groups. One group is provided with Xarelto, and the other one group is provided without any prophylactic antithrombotic. To check the presence of a deep vein thrombosis of the lower limb, bilateral sonographic examinations are arranged for all participants preoperatively and at 3 and 14 days postoperatively. One radiologists who was blinded to the nature of the study interpreted the results of the sonographic examination. The present of pulmonary embolism, DVT-related symptoms, and complications are recorded during the 3-months follow-up in orthopedics outpatients. The symptom which associated with DVT is defined as the signs of leg such as unusual pain, edema, swelling, warm skin, and red or discolored skin. Complications related to Xarelto include major bleeding, infection, and non-healing wound. The expected number of participants in each group is 89, which is calculated by G * Power version 3.1. The intention to treat analysis is used in this study. The investigators compare the incidences of DVT, pulmonary embolism, and complications between the two groups.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Venous Thromboembolism, Arthroplasty
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
178 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Rivaroxaban
Arm Type
Experimental
Arm Description
The participants are provided with Rivaroxaban 10mg
Arm Title
Control
Arm Type
No Intervention
Arm Description
The participants are provided without antithrombotics
Intervention Type
Drug
Intervention Name(s)
Rivaroxaban 10 MG
Other Intervention Name(s)
Xarelto
Intervention Description
Patients are randomly divided into two groups. One group receives no prophylaxis with an anticoagulant, the other one receives Rivaroxaban. The dosage of Rivaroxaban is 10 mg given orally once daily starting on the day of the surgery and continuing the following 13 days.
Primary Outcome Measure Information:
Title
Deep vein thrombosis
Description
The incidence of both asymptomatic and symptomatic deep vein thrombosis
Time Frame
Up to 3 months after THR and TKR
Title
Pulmonary embolism
Description
The incidence of pulmonary embolism
Time Frame
Up to 3 months after THR and TKR
Secondary Outcome Measure Information:
Title
Complication
Description
Major bleeding, infection, and non-healing wound
Time Frame
Up to 3 months after THR and TKR
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Undergo total knee replacement or total hip replacement
Exclusion Criteria:
Recent antithrombotics use
A history of a coagulopathy
Recent thromboembolic disease
Preoperative deep vein thrombosis screening presents positive
Age below 20
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Cheng-Ming Chou
Phone
88652765041
Ext
8297
Email
james58.chou456@msa.hinet.net
Facility Information:
Facility Name
Ditmanson Medical Foundation Chiayi Christian Hospital
City
Chiayi City
ZIP/Postal Code
60002
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Cheng-Ming Chou, MD
Email
James58.chou456@msa.hinet.net
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Xarelto for Thromboprophylaxis After Total Hip and Total Knee Arthroplasty
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