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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04504318
Other study ID # IRB-49355
Secondary ID
Status Recruiting
Phase Phase 1/Phase 2
First received
Last updated
Start date August 12, 2020
Est. completion date August 1, 2024

Study information

Verified date May 2024
Source Stanford University
Contact Arash Momeni, MD
Phone 650-723-6189
Email amomeni@stanford.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Apixaban 2.5 MG Oral Tablet
Patients will be assigned to the respective study groups postoperatively upon arrival in the post-anesthesia care unit. Hence, surgeons are blinded at the time of surgery as to study group assignment. Chemoprophylaxis will continue for the duration of the hospitalization.
Enoxaparin 40Mg/0.4mL Prefilled Syringe
Patients will be assigned to the respective study groups postoperatively upon arrival in the post-anesthesia care unit. Hence, surgeons are blinded at the time of surgery as to study group assignment. Chemoprophylaxis will continue for the duration of the hospitalization.

Locations

Country Name City State
United States Stanford University Medical Center Stanford California

Sponsors (1)

Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome

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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