Comparison Between Low Dose and High Dose Intra-articular Tranexamic Acid in Total Knee Arthroplasty
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ClinicalTrials.gov Identifier: NCT03044041 |
Recruitment Status :
Completed
First Posted : February 6, 2017
Last Update Posted : January 30, 2018
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Blood Loss, Surgical | Drug: Tranexamic Acid | Phase 4 |
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 80 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Triple (Participant, Investigator, Outcomes Assessor) |
Primary Purpose: | Treatment |
Official Title: | Topical Intra‐Articular High Doses Compared With Low Doses of Tranexamic Acid to Reduce Blood Loss in Primary Total Knee Arthroplasty: A Double‐Blind Randomized Controlled Trial |
Actual Study Start Date : | January 2016 |
Actual Primary Completion Date : | January 2017 |
Actual Study Completion Date : | June 2017 |

Arm | Intervention/treatment |
---|---|
Experimental: Low dose
single dose of intra-articular Tranexamic acid 500 miligrams
|
Drug: Tranexamic Acid
IA (intra-articular) tranexamic acid after capsule closure |
Active Comparator: High dose
Single dose of intra-articular Tranexamic acid 3 grams
|
Drug: Tranexamic Acid
IA (intra-articular) tranexamic acid after capsule closure |
- Total blood loss [ Time Frame: 72 hours after TKA ]Blood loos that calculated from Haemoglobin drop at 72 hours after surgery
- Blood transfusion [ Time Frame: 0-72 hours after surgery ]incidence of blood transfusion after surgery
- Rate of participants with thromboembolism [ Time Frame: At 72 hours and 2 weeks after surgery ]Clinical thromboembolism after surgery
- Rate of participants with infection [ Time Frame: 0-3 months after surgery ]Superficial or deep infection after TKA
- Knee ROM [ Time Frame: At 2, 6 weeks after surgery ]Range of motion of the knee
- Functional score [ Time Frame: At 6 weeks after surgery ]Modified WOMAC

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Ages Eligible for Study: | 50 Years to 90 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Osteoarthritic knee who underwent primary total knee arthroplasty
Exclusion Criteria:
- Abnormal coagulation or bleeding disorder
- Allergy to tranexamic acid
- History of thromboembolism or ischemic heart disease or cerebrovascular accident
- chronic kidney disease stage 3-4

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03044041
Thailand | |
Thammasat University | |
Klong Luang, Pathum Thani, Thailand, 12120 |
Responsible Party: | Supakit Kanitnate, Investigator, Thammasat University |
ClinicalTrials.gov Identifier: | NCT03044041 History of Changes |
Other Study ID Numbers: |
OrthoTU08 |
First Posted: | February 6, 2017 Key Record Dates |
Last Update Posted: | January 30, 2018 |
Last Verified: | January 2018 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Undecided |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Blood loss Tranexamic acid Total knee arthroplasty Topical administration |
Hemorrhage Blood Loss, Surgical Pathologic Processes Intraoperative Complications Tranexamic Acid |
Antifibrinolytic Agents Fibrin Modulating Agents Molecular Mechanisms of Pharmacological Action Hemostatics Coagulants |