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Oral and Intravenous Tranexamic Acid in Lumbar Spine Surgery

A Randomized Controlled Trial of Oral and Intravenous Tranexamic Acid in Lumbar Spine Surgery

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03037515
Enrollment
83
Registered
2017-01-31
Start date
2017-02-15
Completion date
2018-07-16
Last updated
2024-02-20

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

Conditions

Blood Loss Anemia, Blood Loss, Surgical

Brief summary

The purpose of this project is to compare the effectiveness of two different but well accepted routes of administration of tranexamic acid in order to reduce blood loss and need for transfusion in patients undergoing lumbar spine surgery. Specifically, this study seeks to identify if intravenous tranexamic acid is superior to oral tranexamic acid in reducing blood loss and need for transfusion.

Detailed description

Spine surgery is associated with large amount of perioperative blood loss. Factors influencing blood loss include surgical technique, operative time, number of vertebral levels arthrodesed, and others. Significant blood loss is associated with complications such as hypotension, end organ damage, or coagulopathy. Blood transfusions can increase risks of infection, blood incompatibility, and allergic reactions. Due to the significant risks and complications associated with blood loss and allogenic transfusions, efforts to identify safe and effective ways of lowering blood loss during spine surgery are crucial. Many methods have been utilized to reduce allogenic blood transfusions, such as autologous blood predonation, antifibrinolytic drugs, acute normovolemic hemodilution, intraoperative blood salvage, and others. Furthermore, the administration of antifibrinolytics, such as tranexamic acid (TXA) and epsilon-aminocaproic acid (EACA), has been shown to reduce bleeding in cardiac, gynecological, urologic and total joint replacement surgeries. There have been many published studies investigating various antifibrinolytic agents such as TXA, EACA, and aprotinin. While aprotinin was shown to increase mortality rate in patients following cardiac surgery, TXA and EACA have not been shown to cause any substantial morbidity or to increase rate of thromboembolic events. Although IV TXA has been shown to be effective in reducing blood loss and transfusions in patients undergoing spine surgery, no studies in the literature have investigated the efficacy of PO TXA in decreasing blood loss and transfusions. The investigators believe that PO TXA will be just as efficacious and more cost-effective in reducing blood loss and transfusion needs in patients undergoing lumbar spine surgery. The ultimate goal is identifying the most cost-effective protocol to decrease blood loss and need for transfusion. If oral TXA is found to be as efficacious as IV TXA in reducing blood loss and need for transfusion, significant cost savings can be achieved for the patient and the health care system in general.

Interventions

DRUGTranexamic Acid

To identify if intravenous tranexamic acid is superior to oral tranexamic acid in reducing blood loss and need for transfusion in lumbar spine surgery.

Sponsors

Henry Ford Health System
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Adult patients over age 18 and scheduled for open lumbar spine surgery (primary or revision) * Must be able to swallow tablets

Exclusion criteria

* Known allergy to TXA * History of renal failure or kidney transplant * History of arterial thromboembolic event (eg. myocardial infarction, stroke) within the past year * Placement of an arterial stent within the past year * History of blood clots (DVT, PE) within the past year * Refusal to receive blood products

Design outcomes

Primary

MeasureTime frameDescription
Intra-operative blood loss between the two groupsDay of surgery to 1 day after surgery, up to 7 daysFor males: BV = 0.3669\*(Height in meters)\^3 + 0.03219\*(Weight in kilograms) + 0.6041 For females: BV = 0.3561\*(Height in meters)\^3 + 0.03308\*(Weight in kilograms) + 0.1833 Hbloss = BV\*(Hbi-Hbe )\*0.001 + Hbt Blood loss = 1000\*(Hbloss/Hbi) Hbloss = Hemoglobin loss; BV = Blood Volume; Hbi = initial Hgb; Hbe = ending Hgb; Hbt = transfused Hgb = about 52g (SD 5.4g) per 1u pRBC (320mL)

Secondary

MeasureTime frame
Post-operative drop in hemoglobin between the two groups1 day after surgery until patient is discharged, up to 7 days
Post-operative blood loss between the two groups1 day after surgery until patient is discharged, up to 7 days
Number of units transfused between the two groups1 day after surgery until patient is discharged, up to 7 days
Post-operative drain output between the two groups1 day after surgery until patient is discharged, up to 7 days
Incidence of thromboembolic events between the two groups1 day after surgery until patient returns for first postoperative visit (through study completion, an average of 4 weeks after surgery)

Countries

United States

Outcome results

None listed

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