LMWH Vs Aspirin for VTE Prophylaxis in Orthopaedic Oncology
Launched by MASSACHUSETTS GENERAL HOSPITAL · Aug 5, 2017
Trial Information
Current as of June 26, 2025
Enrolling by invitation
Keywords
ClinConnect Summary
Lower extremity orthopaedic surgery and malignancy are both known major risk factors for venous thromboembolism (VTE). Guidelines from high quality data exist with regards to VTE prophylaxis in patients undergoing orthopaedic surgery, particularly joint arthroplasty. Far fewer data are available regarding the efficacy of various methods of pharmacologic VTE prophylaxis in patients undergoing surgery for primary or metastatic musculoskeletal malignancies as malignancy itself is known to confer a hypercoagulable state. The existing data, including published data from our institution, are almo...
Gender
ALL
Eligibility criteria
- Patients will first be evaluated for inclusion in a master observational study with the following inclusion criteria:
- • 1. Age ≥18 years
- • 2. Prior or planned surgery on the pelvis or lower extremity
- 3. Fulfills one of the following:
- • a. Cohort A: Metastatic osseous disease, undergoing: i. Endoprosthetic reconstruction ii. Curettage, cement packing, and fixation with nails, plates, and/or screws iii. Intramedullary nail fixation only b. Cohort B: Primary bone sarcoma, undergoing wide resection, amputation, or reconstruction with endoprosthesis, allograft, or allograft-prosthesis composite (APC).
- • c. Cohort C: Primary soft tissue sarcoma ≥5 cm in diameter, undergoing wide resection
- • 4. Anticoagulation therapy was received or is planned.
- • In addition to fulfilling all the inclusion criteria in Part 1 of this study, participants must also not meet any of the below exclusion criteria in order to be eligible for randomization to either aspirin or LMWH.
- Exclusion Criteria:
- • 1. Documented prior history of VTE.
- • 2. Preoperative use of therapeutic or prophylactic chemical anticoagulation at the time of surgery.
- • 3. Documented allergy/adverse reaction to either of the two study drugs.
- • 4. Presence of inferior vena cava (IVC) filter.
- • 5. Known, diagnosed hypercoagulable state (other than malignancy).
- • 6. Inability to receive chemical anticoagulation.
- • 7. Preoperative use of full-strength aspirin 325 mg daily; patients already taking aspirin 81 mg daily will not be excluded.
- • 8. Inability for the patient him/herself to give informed consent due to delirium, dementia, or any other reason.
- • 9. Pregnancy
- • 10. Fear of needles that prevents administration of LMWH.
- • 11. Inability to administer medications via needles.
- • 12. For patients with metastatic osseous disease, a Khorana score of ≥3.
- • Pregnancy testing, via a urine or blood test, is a routine part of pre-operative laboratory testing in patients scheduled to undergo orthopaedic surgeries. Attending surgeons may also choose to exclude any patient from randomization at their discretion.
About Massachusetts General Hospital
Massachusetts General Hospital (MGH) is a leading academic medical center located in Boston, Massachusetts, renowned for its commitment to advancing medical research and patient care. As a prominent teaching hospital affiliated with Harvard Medical School, MGH plays a pivotal role in clinical trials across a wide range of disciplines, including cardiology, oncology, neurology, and more. The institution is dedicated to fostering innovative research that translates into effective therapies and improved health outcomes. MGH's Clinical Trials Office provides comprehensive support to facilitate the design, implementation, and management of clinical studies, ensuring adherence to the highest ethical standards and regulatory compliance. With a focus on collaboration and patient-centered care, MGH strives to enhance medical knowledge and contribute to the future of healthcare.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Baltimore, Maryland, United States
Boston, Massachusetts, United States
Boston, Massachusetts, United States
Tampa, Florida, United States
Cleveland, Ohio, United States
Camden, New Jersey, United States
Boston, Massachusetts, United States
Los Angeles, California, United States
New Orleans, Louisiana, United States
Columbia, Missouri, United States
Patients applied
Trial Officials
Santiago A Lozano-Calderon, MD, PhD
Principal Investigator
Massachusetts General Hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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