The Use of Tranexamic Acid to Reduce Blood Loss in Acetabular Surgery
TXA
1 other identifier
interventional
87
1 country
2
Brief Summary
The purpose of this study is to determine if patients undergoing acetabular ORIF (open reduction with internal fixation) who receive tranexamic acid have a reduced risk of allogenic blood transfusion, perioperative blood loss, wound complication and higher risk for thromboembolic events compared to patients who receive placebo. Investigators want to determine the cost-effectiveness related to allogenic blood transfusion as a blood loss management strategy in acetabular open reduction internal fixation (ORIF). Orthopaedic surgery carries with it a significant risk for blood loss. Current management of perioperative blood loss is the use of allogenic blood transfusion. Allogenic blood transfusion carries with it a risk for HIV and Hepatitis C as well as multiple adverse reactions. There have been significant efforts to reduce the use of allogenic blood transfusion in orthopaedic surgery. Tranexamic acid, an anti-fibrinolytic agent, has been used in management of blood during surgery. In order to determine the impact of tranexamic acid in reducing blood loss among patients undergoing acetabular ORIF, investigators will conduct a prospective randomized study. Patients undergoing acetabular surgery will be screened for this study. Patients will be then randomized to placebo or tranexamic acid which will be administered during and after surgery. The following data will be collected: patient characteristics, surgery information, blood loss, blood transfusions, wound complication within 30 days of surgery, and cost.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_3
Started Oct 2012
Longer than P75 for phase_3
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2012
CompletedFirst Submitted
Initial submission to the registry
February 11, 2016
CompletedFirst Posted
Study publicly available on registry
February 18, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 25, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
July 25, 2017
CompletedResults Posted
Study results publicly available
January 19, 2021
CompletedApril 21, 2022
January 1, 2021
3.8 years
February 11, 2016
February 5, 2018
April 19, 2022
Conditions
Outcome Measures
Primary Outcomes (2)
Allogenic Blood Transfusion Rates
Number of participant received allogenic blood transfusions.
post-operative
Units of Packed Red Blood Cells Transfused
Average units packed red blood cells transfused among participants
perioperative
Secondary Outcomes (2)
Number of Participants With a Thromboembolic Event
30 days
Estimate Blood Loss
perioperative
Study Arms (2)
Placebo
PLACEBO COMPARATORInactive
Tranexamic
ACTIVE COMPARATORTranexamic acid: anti-fibrinolytic agents
Interventions
Tranexamic acid: anti-fibrinolytic agents
Eligibility Criteria
You may qualify if:
- All patients aged 18 or above undergoing acetabular ORIF.
You may not qualify if:
- All patients aged below 18 years undergoing acetabulum surgery
- Patients with color-blindness (color vision changes used to assess toxicity)
- Patients with subarachnoid hemorrhage.
- Patients with active intravascular coagulation.
- Patients with a previous history of venous thromboembolism or with a history of hypercoaguable conditions (i.e. Factor V Leiden, antiphospholipid antibody).
- Prisoners
- Pregnant women
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
University of Missouri
Columbia, Missouri, 65212, United States
Carolinas Medical Center
Charlotte, North Carolina, 28205, United States
Related Publications (40)
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PMID: 19926634BACKGROUND
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Results Point of Contact
- Title
- Rachel Seymour, PhD
- Organization
- CarolinasHS
Study Officials
- PRINCIPAL INVESTIGATOR
Madhav Karunakar, MD
Wake Forest University Health Sciences
Publication Agreements
- PI is Sponsor Employee
- Yes
Study Design
- Study Type
- interventional
- Phase
- phase 3
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 11, 2016
First Posted
February 18, 2016
Study Start
October 1, 2012
Primary Completion
July 25, 2016
Study Completion
July 25, 2017
Last Updated
April 21, 2022
Results First Posted
January 19, 2021
Record last verified: 2021-01