Venous Thromboembolism Clinical Trial
Official title:
A Randomized Controlled Trial Comparing Apixaban Versus Enoxaparin Following Microsurgical Breast Reconstruction
Subcutaneous enoxaparin is currently the gold standard for VTE chemoprophylaxis. However, the efficacy of chemoprophylaxis with subcutaneous enoxaparin is affected by patient-level factors, thus, resulting in VTE events despite guideline-compliant prophylaxis. A population at particular risk is the growing number of patients who undergo autologous breast reconstruction. Direct oral anticoagulants (DOAC) might be a less invasive, yet, more efficacious mode of chemoprophylaxis in this patient population. Hence, the proposed work has the potential to cause a paradigm shift in chemoprophylaxis guidelines in a large population of patients undergoing plastic surgery.
Status | Recruiting |
Enrollment | 106 |
Est. completion date | August 1, 2024 |
Est. primary completion date | August 1, 2024 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 89 Years |
Eligibility | Inclusion Criteria: - Adult (>18 years) women - Scheduled to undergo unilateral or bilateral microsurgical breast reconstruction with free abdominal flaps (i.e. muscle-sparing transverse rectus abdominis musculocutaneous [TRAM] and/or deep inferior epigastric artery perforator [DIEP]) flap) - Caprini score of 6 or greater. - Ability to understand and the willingness to sign a written informed consent document. Exclusion Criteria: - Contraindication to the use of apixaban or enoxaparin - Active bleeding - History of bleeding disorder - History of coagulopathy - History of heparin-induced thrombocytopenia - History of liver disease - History of renal disease (creatinine clearance <30 mL/min; serum creatinine >1.6 mg/dL) - Major neurosurgical intervention (brain/spine) within the past 90 days - Ophthalmologic procedure within the past 90 days - Uncontrolled hypertension - History of alcohol and/or substance abuse - Need for therapeutic anticoagulation - Pregnant or Nursing |
Country | Name | City | State |
---|---|---|---|
United States | Stanford University Medical Center | Stanford | California |
Lead Sponsor | Collaborator |
---|---|
Stanford University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Apixaban vs. Enoxaparin - Bleeding event | To examine the rate of bleeding events in patients receiving oral apixaban versus subcutaneous enoxaparin following microsurgical breast reconstruction | 90-day events | |
Secondary | Apixaban vs. Enoxaparin - Venous Thromboembolism (VTE) event | To examine the rate of VTE events in patients receiving oral apixaban versus subcutaneous enoxaparin following microsurgical breast reconstruction | 90-day events |
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