RecruitingNCT07309848

Hip Fracture Surgery Timing and Blood Transfusion Risk in Patients on DOACs

Blood Transfusion Risk After Early vs. Delayed Surgery in Hip Fracture Patients on Direct Oral Anticoagulants: A Natural Experiment


Sponsor

St. Antonius Hospital

Enrollment

374 participants

Start Date

Nov 1, 2025

Study Type

OBSERVATIONAL

Summary

This study looks at patients with hip fractures who are taking direct oral anticoagulants (DOACs), a type of blood thinner. In many hospitals, surgery for these patients is delayed because of concerns about bleeding, but waiting longer can also increase risks such as complications and longer hospital stays. The purpose of this study is to find out whether operating within 24 hours is as safe as delaying surgery beyond 24 hours. Specifically, the investigators want to know if early surgery does not lead to a higher need for blood transfusions compared to delayed surgery.


Eligibility

Inclusion Criteria2

  • Isolated hip fracture classified as AO/OTA 31A or 31B requiring surgical intervention.
  • Current DOAC use with the last dose taken ≤24 hours before emergency department (ED) presentation

Exclusion Criteria5

  • Pathologic or periprosthetic hip fractures.
  • Fracture sustained >24 hours before ED presentation.
  • Inter-hospital transfer.
  • Hematologic disorders (e.g., thalassemia, sickle cell disease, aplastic anemia, myelodysplastic syndromes, leukemia).
  • Use of a non-EMA-approved DOAC (e.g., betrixaban).

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Locations(7)

Ziekenhuisgroep Twente Hospital

Almelo, Netherlands

Onze Lieve Vrouw Gasthuis Hospital

Amsterdam, Netherlands

Rijnstate Hospital

Arnhem, Netherlands

Deventer Hospital

Deventer, Netherlands

Martini Hospital

Groningen, Netherlands

Diakonessenhuis Hospital

Utrecht, Netherlands

St. Antonius Hospital

Utrecht, Netherlands

View Full Details on ClinicalTrials.gov

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NCT07309848