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Reduced-Dose Apixaban and Rivaroxaban Versus Low-Molecular-Weight Heparin in Patients With Hematologic Malignancies

Study acronym: HEM-DOAC
StatusRecruiting
PhaseNot applicable
Started
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Record status
This record was last updated December 26, 2025 (before its estimated April 30, 2026 completion). Its status may not reflect the trial's current state.

Record History

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  1. Minor Study title shortened, about 8 wordsv2
  2. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
2,948 trials monitored
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1,261 trials monitored
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and 1 more disease
This study investigates the efficacy and safety of direct oral anticoagulants (DOACs) in comparison with standard low-molecular-weight heparin (LMWH) for the prevention of venous thromboembolism in patients with hematological malignancies. Eligible participants will be randomized to receive reduced-dose apixaban, reduced-dose rivaroxaban, or standard-dose LMWH. The primary objective is to evaluate the incidence of venous thromboembolism during a 6-month follow-up period. Secondary objectives include assessment of bleeding complications, overall survival, and treatment adherence. The results of this study may provide evidence for safer and more convenient thromboprophylaxis strategies in patients with blood cancers.
Trial Details
NCT Number NCT07270263
Lead Sponsor Medical University of Gdansk
Conditions
(from sponsor)
Lymphoma, Leukemia, Multiple Myeloma (MM), Lymphoma, Large B-Cell, Diffuse (DLBCL), Lymphoma, Venous Thromboembolic Disease, VTE (Venous Thromboembolism), PE - Pulmonary Embolism, Hematologic Malignacies
Related terms Hematologic Neoplasms, Leukemia, Lymphoma, Multiple Myeloma, Pulmonary Embolism, Venous Thromboembolism
Enrollment 100 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov