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Tranexamic Acid Use in Acute Hip Fractures

Primary Purpose

Acute Hip Fractures

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Tranexamic Acid
Placebo
Sponsored by
Carilion Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Hip Fractures focused on measuring Hemiarthroplasty, Intramedullary nail, Tranexamic acid, Transfusion

Eligibility Criteria

65 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Geriatric patients age 65 or older who require surgery for a low energy trauma hip fracture

Exclusion Criteria:

  • Prothrombotic state
  • Cardiac stent within the past year with corresponding antiplatelet therapy
  • Mechanical heart valves
  • Deep vein thrombosis history
  • Aortic stenosis
  • Currently on Coumadin
  • Malignancy
  • Kidney dialysis
  • Non-English speaking patients
  • Medications contraindicated with tranexamic acid.

Sites / Locations

  • Carilion Roanoke Memorial Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Placebo Comparator

Experimental

Experimental

Placebo Comparator

Arm Label

Hemiarthroplasty - Placebo

Intramedullary nail - Tranexamic Acid

Hemiarthroplasty - Tranexamic Acid

Intramedullary nail - Placebo

Arm Description

Patients are placed into this arm based on the type of surgery performed and are randomized to receive placebo

Patients are placed into this arm based on the type of surgery performed and are randomized to receive tranexamic acid

Patients are placed into this arm based on the type of surgery performed and are randomized to receive tranexamic acid

Patients are placed into this arm based on the type of surgery performed and are randomized to receive placebo

Outcomes

Primary Outcome Measures

Transfusion reduction rate
Determine the efficacy of Tranexamic Acid (TXA) in the reduction of allogenic blood transfusion within 1 week following either hemiarthroplasty or intramedullary nailing for intertrochanteric fracture.

Secondary Outcome Measures

Tranexamic acid post operative complications
Determine what effect TXA has on post-operative complications within 1 year following surgery for either hemiarthroplasty or intramedullary nailing for intertrochanteric fracture.

Full Information

First Posted
October 13, 2016
Last Updated
February 7, 2023
Sponsor
Carilion Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT02947529
Brief Title
Tranexamic Acid Use in Acute Hip Fractures
Official Title
The Use of Tranexamic Acid to Reduce the Need for Transfusion 1 Week Post-operatively for Hemiarthroplasty or Intramedullary Nailing Needed to Correct Acute Hip Fractures
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
August 2015 (Actual)
Primary Completion Date
February 4, 2022 (Actual)
Study Completion Date
May 22, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Carilion Clinic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
BACKGROUND: Tranexamic acid (TXA) has been used widely for the reduction of post operative blood loss for various orthopaedic procedures including but not limited to total hip arthroplasty and total knee arthroplasty. A recent multihospital meta-analysis conducted in 2013 showed that patients who received TXA showed a significant reduction in post-operative transfusion (20.1% to 7.7%). The procedures the investigators will be evaluating are the intramedullary nail for intertrochanteric fracture and hip hemiarthroplasty. These procedures are similar to the total hip or knee replacement in that they can result in significant blood loss that requires a post operative transfusion. STUDY PURPOSE: To determine the efficacy of TXA to decrease the rate of post-operative transfusion for acute hip fractures repaired with the following two methods, intramedullary nailing for intertrochanteric fracture and hemiarthroplasty. METHODS: The model for the study is a prospective randomized control trial. Patients will be placed in one of two arms of the study after passing our inclusion criteria. The arms will be for either the intramedullary nailing for intertrochanteric fracture or for hemiarthroplasty. These two categories will be subdivided into those receiving TXA and those not receiving TXA. The patients in each category will have standard post-operative care and laboratory testing. The investigators will record the patients in either arm of the study, whether it be no TXA or TXA, who require post-operative transfusion within 1 week of the operation.
Detailed Description
This is a prospective randomized control trial. Patients scheduled for either intramedullary nailing for intertrochanteric fractures or for hemiarthroplasty will be selected for the study population. The proposed research is needed to bridge the gap between the efficacy of TXA in elective, non-emergency procedures (such as total knee arthoplasty and total hip arthroplasty) and its efficacy in emergent acute hip fracture interventions. This study will use intravenous TXA (1g pre-op and 1g post-op) to study its effect on both the reduction of blood loss during intramedullary nail for intertrochanteric fractures and hemiarthroplasty procedures, and the subsequent reduction in the rate of blood transfusion in this patient population. Both study and control groups will have standard post-operative care and laboratory testing and will be followed for one year post-operatively to record adverse events.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Hip Fractures
Keywords
Hemiarthroplasty, Intramedullary nail, Tranexamic acid, Transfusion

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Subjects undergoing surgery for acute hip fractures with a long trochanteric femoral nail (TFN) or hemiarthroplasty will randomized 50:50 to receive 1 dose of either tranexamic acid (TXA) or saline placebo solution prior to surgery and 1 dose during wound closure.
Masking
ParticipantInvestigator
Masking Description
Both the participants and the operating surgeons, who are members of the investigative team, will be blinded to which study group the participant is in throughout the study period.
Allocation
Randomized
Enrollment
113 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Hemiarthroplasty - Placebo
Arm Type
Placebo Comparator
Arm Description
Patients are placed into this arm based on the type of surgery performed and are randomized to receive placebo
Arm Title
Intramedullary nail - Tranexamic Acid
Arm Type
Experimental
Arm Description
Patients are placed into this arm based on the type of surgery performed and are randomized to receive tranexamic acid
Arm Title
Hemiarthroplasty - Tranexamic Acid
Arm Type
Experimental
Arm Description
Patients are placed into this arm based on the type of surgery performed and are randomized to receive tranexamic acid
Arm Title
Intramedullary nail - Placebo
Arm Type
Placebo Comparator
Arm Description
Patients are placed into this arm based on the type of surgery performed and are randomized to receive placebo
Intervention Type
Drug
Intervention Name(s)
Tranexamic Acid
Other Intervention Name(s)
TXA
Intervention Description
intravenous dose
Intervention Type
Other
Intervention Name(s)
Placebo
Other Intervention Name(s)
Saline
Intervention Description
intravenous dose
Primary Outcome Measure Information:
Title
Transfusion reduction rate
Description
Determine the efficacy of Tranexamic Acid (TXA) in the reduction of allogenic blood transfusion within 1 week following either hemiarthroplasty or intramedullary nailing for intertrochanteric fracture.
Time Frame
1 week
Secondary Outcome Measure Information:
Title
Tranexamic acid post operative complications
Description
Determine what effect TXA has on post-operative complications within 1 year following surgery for either hemiarthroplasty or intramedullary nailing for intertrochanteric fracture.
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Geriatric patients age 65 or older who require surgery for a low energy trauma hip fracture Exclusion Criteria: Prothrombotic state Cardiac stent within the past year with corresponding antiplatelet therapy Mechanical heart valves Deep vein thrombosis history Aortic stenosis Currently on Coumadin Malignancy Kidney dialysis Non-English speaking patients Medications contraindicated with tranexamic acid.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Trevor Owen, MD
Organizational Affiliation
Carilion Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Carilion Roanoke Memorial Hospital
City
Roanoke
State/Province
Virginia
ZIP/Postal Code
24014
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
25116268
Citation
Poeran J, Rasul R, Suzuki S, Danninger T, Mazumdar M, Opperer M, Boettner F, Memtsoudis SG. Tranexamic acid use and postoperative outcomes in patients undergoing total hip or knee arthroplasty in the United States: retrospective analysis of effectiveness and safety. BMJ. 2014 Aug 12;349:g4829. doi: 10.1136/bmj.g4829.
Results Reference
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Tranexamic Acid Use in Acute Hip Fractures

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