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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06244498
Other study ID # 01
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2018
Est. completion date December 31, 2022

Study information

Verified date February 2024
Source Podkarpackie Oncological Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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


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.


Recruitment information / eligibility

Status Completed
Enrollment 110
Est. completion date December 31, 2022
Est. primary completion date December 31, 2021
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Patological fracture - Arthroplasty using a modular prosthesis. Exclusion Criteria: - threatened fracture - intraoperative blood transfusion - fracture fixation

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
Poland SzSPOO Brzozów Brzozów Podkarpackie

Sponsors (1)

Lead Sponsor Collaborator
Piotr Biega

Country where clinical trial is conducted

Poland, 

References & Publications (1)

CRASH-2 collaborators; Roberts I, Shakur H, Afolabi A, Brohi K, Coats T, Dewan Y, Gando S, Guyatt G, Hunt BJ, Morales C, Perel P, Prieto-Merino D, Woolley T. The importance of early treatment with tranexamic acid in bleeding trauma patients: an explorator — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Number of participants who require a blood transfusion. Need of blood transfusion During Hospitalization (up to day 10)
Secondary Estimeted blood lost after surgery. Gross total blood loss was estimated utilizing the formula PBV × (Hctpre- Hctpost)/Hcta During Hospitalization (up to day 3)
Secondary Number of participants with embolic complication. Yes or No During Hospitalization (up to day 10)
See also
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