drugset / Trial / NCT07270263

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

NCT07270263

Recruiting 100 enrolled Medical University of Gdansk
RandomizedParallel-groupOpen-labelPrevention

Summary

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.

Timeline

Start
2024-11-22
Primary completion
2026-04-30
Completion
2026-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Apixaban Small molecule 2.5 mg Oral
Comparator Enoxaparin sodium Other / unclassified 40 mg Subcutaneous
Subject Rivaroxaban Other / unclassified 10 mg Oral