Xarelto for Thromboprophylaxis After Total Hip and Total Knee Arthroplasty

Sponsor
Chiayi Christian Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05449327
Collaborator
(none)
178
1
2
17.2
10.3

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Drug: Rivaroxaban 10 MG
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
178 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Xarelto for Thromboprophylaxis After Total Hip and Total Knee Arthroplasty
Anticipated Study Start Date :
Jul 25, 2022
Anticipated Primary Completion Date :
Nov 30, 2023
Anticipated Study Completion Date :
Dec 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Rivaroxaban

The participants are provided with Rivaroxaban 10mg

Drug: Rivaroxaban 10 MG
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.
Other Names:
  • Xarelto
  • No Intervention: Control

    The participants are provided without antithrombotics

    Outcome Measures

    Primary Outcome Measures

    1. Deep vein thrombosis [Up to 3 months after THR and TKR]

      The incidence of both asymptomatic and symptomatic deep vein thrombosis

    2. Pulmonary embolism [Up to 3 months after THR and TKR]

      The incidence of pulmonary embolism

    Secondary Outcome Measures

    1. Complication [Up to 3 months after THR and TKR]

      Major bleeding, infection, and non-healing wound

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Ditmanson Medical Foundation Chiayi Christian Hospital Chiayi City Taiwan

    Sponsors and Collaborators

    • Chiayi Christian Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Chiayi Christian Hospital
    ClinicalTrials.gov Identifier:
    NCT05449327
    Other Study ID Numbers:
    • IRB2021079
    First Posted:
    Jul 8, 2022
    Last Update Posted:
    Jul 14, 2022
    Last Verified:
    Jul 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    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
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 14, 2022