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Search / Trial NCT03244020

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.

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

0 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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