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Comparison on the Effectiveness of Regimens with Combination of Intravenous and Intra-articular Applications of Tranexamic Acid for the Significant Reduction of Blood Loss in Primary Knee Osteoarthritis undergoing Total Knee Arthroplasty: A Randomized Clinical Trial Study

Comparison on the Effectiveness of Regimens with Combination of Intravenous and Intra-articular Applications of Tranexamic Acid for the Significant Reduction of Blood Loss in Primary Knee Osteoarthritis undergoing Total Knee Arthroplasty: A Randomiz

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20170503003
Enrollment
90
Registered
2017-05-03
Start date
2015-10-01
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

blood loss after total knee arthroplasty blood transfusion rate blood loss

Interventions

regimen 1. 10&#45
15mg/kg/dose up to 1g maximum tranexamic acid will be given intravenously 15&#45
20 minutes before incision&#44
1g tranexamic acid mixed with 20ml NSS will be introduced intra&#45
articularly after joint capsule closure&#44
20ml NSS will be given intravenously 3 hours after operation.,regimen 2. 10&#45
15mg/kg/dose up to 1g maximum tranexamic acid mixed with NSS total of 20 ml will be given intravenously 3 hours after operation
Active Comparator Drug,Active Comparator Drug
Tranexamic Acid,Tranexamic Acid

Sponsors

None
Lead Sponsor

Eligibility

Sex/Gender
All
Age
55 Years to 85 Years

Inclusion criteria

Inclusion criteria: &#45; Primary osteoarthritis &#45; 55&#45;85 years of age &#45; Platelet count of more than 100&#44;000 &#45; PT&#44;PTT&#44;INR (<1.5) within normal limits &#45; Cr < 1.5

Exclusion criteria

Exclusion criteria: &#45; Patients with known genetic or acquired coagulation disorder &#45; Patients with renal failure&#44; liver failure&#44; heart failure&#44; lung failure &#45; Allergy to TXA &#45; Patients with ischemic heart disease or arrhythmia &#45; Previous history of DVT&#44; PE&#44; Stroke &#45; Patient with secondary arthritis &#45; Active infection&#44; Cancer&#44; stroke

Design outcomes

Primary

MeasureTime frame
blood loss post operative mg/dl&#44; ml&#44; %/ blood sample from patient

Secondary

MeasureTime frame
blood transifusion rate post operative ml&#44; Unit/ sample from patient

Countries

Thailand

Contacts

Public Contactketirath rochanaroon

Lerdsin Hospital

prochanaroon@yahoo.com0851623174

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026