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Tranexamic Acid After Pathological Fracture Treated With Modular Arthroplasty

Tranexamic Acid After Pathological Fracture Treated With Modular Arthroplasty: Retrospective Observational Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06244498
Enrollment
110
Registered
2024-02-06
Start date
2018-01-01
Completion date
2022-12-31
Last updated
2024-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metastases to Bone

Keywords

Blood Transfusion, Neoplasm Metastasis, Bone

Brief summary

This study assesses the safety and efficacy of TXA for patients treated for pathological femur fractures using modular prosthetics.

Detailed description

Tranexamic acid is an efficacious medication for curtailing blood loss, haemoglobin drop, and the requirement for transfusions. Additionally, it is a secure medication, even when administered to oncology patients receiving reduction haemarthroplasty for pathological femoral fractures.

Interventions

DRUGTranexamic acid injection

Tranexamic acid were administered at a dose of 1.0 g during the induction of anaesthesia and immediately after surgery.

Sponsors

Piotr Biega
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patological fracture * Arthroplasty using a modular prosthesis.

Exclusion criteria

* threatened fracture * intraoperative blood transfusion * fracture fixation

Design outcomes

Primary

MeasureTime frameDescription
Number of participants who require a blood transfusion.During Hospitalization (up to day 10)Need of blood transfusion

Secondary

MeasureTime frameDescription
Estimeted blood lost after surgery.During Hospitalization (up to day 3)Gross total blood loss was estimated utilizing the formula PBV × (Hctpre- Hctpost)/Hcta
Number of participants with embolic complication.During Hospitalization (up to day 10)Yes or No

Countries

Poland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026