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Clinical Trials/NCT02030821
NCT02030821CompletedPhase 4

TXA (Tranexamic Acid) vs. Amicar (Aminocaproic Acid) in Total Knee and Hip Arthroplasty- Effectiveness, Safety, and Cost Analysis

Duke University1 site in 1 country246 target enrollmentStarted: January 2015Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 4
Status
Completed
Enrollment
246
Locations
1
Primary Endpoint
Total Blood Loss Over Course of Stay (Intraoperative and Postoperatively Until Discharge)

Study Overview

Brief Summary

The purpose of this study is to determine the relative effectiveness of two drug agents, Tranexamic acid (TXA) and aminocaproic acid (Amicar), that act through a similar mechanism of action. These agents are used to decrease blood loss that is a result of major surgery, like total joint arthroplasty. A secondary goal will be investigate the cost-analysis of total hospitalization. Both TXA and Amicar are both currently used in the care of patients undergoing total joint arthroplasty.

Subjects will be randomly assigned to the TXA or Amicar arm. All data needed for this study including blood loss, need for transfusion, preoperative and lowest postoperative hematocrit and hemoglobin, and complications will be collected during the hospitalization stay.

Our Hypothesis is that TXA and Amicar will have similar effectiveness in preventing intraoperative blood loss and the need for transfusion post-op than Amicar.

A detailed cost analysis will show that the overall cost of performing the operative procedure, including transfusions, OR time, and total costs associated with admission cost will be more decreased with Amicar as compared to TXA.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients electing to undergo primary total hip or knee arthroplasty

Exclusion Criteria

  • History of stents
  • Myocardial infarction,
  • Cerebrovascular accident or stroke
  • Deep venous thrombus
  • Pulmonary embolus
  • Late onset color blindness
  • Hypercoagulable state

Arms & Interventions

Tranexamic Acid (TXA)

Active Comparator

TXA will be administered as a 1 gm dose IV prior to the procedure then as a repeat dose of 1 gram at the time of wound closure. These doses are currently used at Duke for Total Knee Arthroplasties (TKAs) and Total Hip Arthroplasties (THAs) per standard of care by the orthopaedic team.

All data needed for this study including blood loss, need for transfusion, preoperative and lowest postoperative hematocrit and hemoglobin, and complications will be collected during the hospitalization.

Intervention: TXA (Drug)

Epsilon-aminocaproic acid (Amicar)

Active Comparator

Administered 5g in 250mL of IV normal saline over 15 minutes prior to the procedure and then an infusion of 5g at the time of wound closure. These doses are currently used at Duke for Total Knee Arthroplasties (TKAs) and Total Hip Arthroplasties (THAs) per standard of care by the orthopaedic team.

All data needed for this study including blood loss, need for transfusion, preoperative and lowest postoperative hematocrit and hemoglobin, and complications will be collected during the hospitalization.

Intervention: Amicar (Drug)

Outcomes

Primary Outcomes

Total Blood Loss Over Course of Stay (Intraoperative and Postoperatively Until Discharge)

Time Frame: Participants will be followed for the duration of hospital stay, an expected average of 5 days

Number of Transfusions

Time Frame: Participants will be followed for the duration of hospital stay, an expected average of 5 days

Difference in Preoperative and Lowest Postoperative Hemoglobin

Time Frame: Participants will be followed for the duration of hospital stay, an expected average of 5 days

Secondary Outcomes

  • Length of Hospitalization Stay(Participants will be followed for the duration of hospital stay, an expected average of 5 days)
  • Cost of Hospitalization(Participants will be followed for the duration of hospital stay, an expected average of 5 days)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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