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Clinical Trials/NCT01980355
NCT01980355CompletedNot Applicable

The Effect of Tranexamic Acid on Blood Loss and Transfusion Rates in Major Oncologic Surgery

Spectrum Health Hospitals1 site in 1 country76 target enrollmentStarted: June 12, 2012Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
76
Locations
1
Primary Endpoint
Number of Participants Who Required Transfusion

Study Overview

Brief Summary

Major surgery can result in blood loss that can require a blood transfusion during and/or after surgery. Tranexamic acid is a medication that was first introduced in the 1960s as a treatment for heavy menstrual bleeding. Over the past 20 years it has been used and studied in patients undergoing open-heart surgery, liver transplantation, and urologic surgery. We believe tranexamic acid may possibly decrease bleeding related to major surgery, resulting in reduced blood loss, lower blood transfusion rates, and possibly decreased hospital costs related to your surgical hospital stay.

In this study, you will receive either the drug tranexamic acid or a placebo. The placebo looks like the tranexamic acid, but does not have any active ingredient in it. The treatment you get will be chosen by chance, like flipping a coin. You will have equal chance of being given the tranexamic acid or the placebo. In this study, both the tranexamic acid and the placebo are considered research.

Detailed Description

Neither you nor the study doctor will choose what treatment you get. You will have an equal chance of being given the tranexamic acid or the placebo. Neither you nor the study doctor will know which treatment you are getting.

You will receive one 1000 mg dose of either tranexamic acid or placebo immediately before surgery. This dose of tranexamic acid or placebo will be given in your vein over 15 minutes.

Information from your medical record related to your surgery and recovery time in the hospital will be collected by medical staff assisting with this study and recorded on study forms. These study forms will be labeled with your study number instead of your name. Additionally, if you return to the hospital within 90 days after you went home from the hospital, information about that hospital visit(s) will also be collected from your medical record.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Eligibility Criteria

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

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

Tranexamic Acid

Experimental

1000mg tranexamic acid; given over 15 minutes into the vein once prior to surgery.

Intervention: Tranexamic Acid (Drug)

Placebo

Placebo Comparator

Placebo given over 15 minutes into the vein once prior to surgery.

Intervention: Placebo (Other)

Outcomes

Primary Outcomes

Number of Participants Who Required Transfusion

Time Frame: From time of surgery to 90 days post hospital discharge

To determine the impact of perioperative administration of tranexamic acid on blood loss and transfusion rates in major oncologic surgery

Secondary Outcomes

  • Estimated Blood Loss(From time of surgery to 90 days post hospital discharge)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Gerald P. Wright

Surgical Oncology and Hepatopancreaticobiliary Surgeon

Spectrum Health Hospitals

Study Sites (1)

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