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Clinical Trials/NCT03483181
NCT03483181
Unknown
Not Applicable

Thromboprophylaxis in Patients Undergoing Orthopedic Surgeries; Using Propensity Score Matching

Hanoi Medical University1 site in 1 country4,000 target enrollmentJanuary 1, 2018

Overview

Phase
Not Applicable
Intervention
Xarelto (rivaroxaban)
Conditions
Thrombosis
Sponsor
Hanoi Medical University
Enrollment
4000
Locations
1
Primary Endpoint
Deep-vein thrombosis (DVT)
Last Updated
8 years ago

Overview

Brief Summary

Venous thromboembolism (VTE), including deep vein thrombosis (DVT) and pulmonary embolism (PE), is a common post-operative complication. The necessity for anticoagulant therapy after orthopedic surgeries is widely understood, but treatment administration patterns in the prevention of venous thromboembolism (VTE) after orthopedic surgeries during the hospital stay have yet to be examined.

The main objective of this study is to perform a comparative effectiveness review examining the benefits and harms associated with venous thromboembolism prophylaxis in patients undergoing orthopedic surgeries.

It is around efficacy and safety evaluation of using anticoagulant for thromboprophylaxis in patients undergoing orthopedic surgeries taking into the account the reliable selection of patients most benefit.

The aims of this study is to analyze patient records in teaching hospitals database of our country (including: Hanoi Medical University, Bach Mai Hospital, Cho Ray Hospital, Viet Duc University Hospital) and compare the outcomes and costs between different types of anticoagulant medications that were prescribed for the prevention of VTE following orthopedic surgeries. This analysis will assess and quantify the outcomes, resource utilization, and cost of care for patients receiving rivaroxaban or enoxaparin. The outcomes of interest include the occurence of DVT and PE, rates of major bleeds, medical resource utilization, and total costs (medical plus pharmacy).

Registry
clinicaltrials.gov
Start Date
January 1, 2018
End Date
December 31, 2018
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Hanoi Medical University
Responsible Party
Principal Investigator
Principal Investigator

Bui My Hanh

Director, Science Research and International Cooperation Unit

Hanoi Medical University

Eligibility Criteria

Inclusion Criteria

  • Undergo Orthopedic Surgery
  • Thromboprophylaxis Decision Taken
  • At least 18 years of age

Exclusion Criteria

  • Planned intermittent pneumatic compression
  • A requirement for anticoagulant therapy that could not be stopped
  • Severe hypersensitivity reaction (eg, anaphylaxis) to rivaroxaban or enoxaparin.
  • Received another anticoagulant for more than 24 hours
  • Active bleeding or a high risk of bleeding
  • Thrombocytopenia associated with a positive test for antiplatelet antibody.
  • Warfarin associated international normalized ratio (INR) more than 1.5 on the day of the surgery
  • Conditions preventing bilateral venography
  • Intensive care unit (ICU) stay after surgery
  • Pregnant or breast-feeding

Arms & Interventions

Orthopedic surgery patient records

Medical records from patients aged 18 years or older with orthopedic surgeries during the hospitalization

Intervention: Xarelto (rivaroxaban)

Orthopedic surgery patient records

Medical records from patients aged 18 years or older with orthopedic surgeries during the hospitalization

Intervention: Lovenox (enoxaparin)

Outcomes

Primary Outcomes

Deep-vein thrombosis (DVT)

Time Frame: 1 year

The frequency of Deep-vein thrombosis Symptoms and signs of DVT may include unilateral leg swelling, pain in the affected leg, calf tenderness in affected leg, increased leg warmth, erythema of affected leg, or a "palpable cord" may be felt in the affected leg.

Mean length of hospital stay in days

Time Frame: 1 year

Length of hospital stay was obtained from the discharge record and was defined as the number of days from patient admission to the hospital for orthopaedic surgeries until discharge from the hospital.

Total cost of care for index hospitalization in Vietnamese dong (VND)

Time Frame: 1 year

The mean total costs (medical plus pharmacy costs) from patient records in each antithrombotic cohort from the index hospitalization

Death

Time Frame: 1 year

Death from any cause including venous thromboembolism

Non-fatal pulmonary embolism (PE)

Time Frame: 1 year

Frequency of pulmonary embolism (non-fatal) Regarding Pulmonary Embolism (PE), diagnosis is suspected in patients with dyspnea, tachypnea, pleuritic chest pain, cough, and/or fever. Diagnosis begins with initial risk stratification "Wells Clinical Model for Evaluating the Pretest Probability of pulmonary embolism (PE) " based on presence of shock or persistent hypotension to identify patients at high risk of early mortality.

Secondary Outcomes

  • Major bleeding risk(After 4 hours of the first dose and up to 2 days after the last dose of the study drug)
  • Other on-treatment bleeding(After 4 hours of the first dose and up to 2 days after the last dose of the study drug)

Study Sites (1)

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