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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
Chiayi Christian Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Venous Thromboembolism

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

First Posted
June 29, 2022
Last Updated
October 2, 2023
Sponsor
Chiayi Christian Hospital
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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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