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Blood Loss Reduction: Effect of Tranexamic Acid Routes in Different Knee Prosthesis: A Randomized Controlled Trial.

Blood Loss Reduction: Effect of Tranexamic Acid Routes in Different Knee Prosthesis: A Randomized Controlled Trial.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20170618001
Enrollment
Unknown
Registered
2017-06-18
Start date
2015-01-30
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Patients with primary osteoarthritis knee scheduled for unilateral primary total knee arthroplasty (TKA) Primary TKA&#44

Interventions

box knee prosthesis without TXA (tranexamic acid) administration. A control group.,Closed&#45
box knee prosthesis with intravenous (IV) TXA administration.,Closed&#45
box knee prosthesis with intra&#45
articular (IA) TXA administration.,Open&#45
box knee prosthesis without TXA (tranexamic acid) administration. A control group.,Open&#45
articular (IA) TXA administration.
No Intervention No treatment,Active Comparator Procedure/Surgery,Active Comparator Procedure/Surgery,No Intervention No treatment,Active Comparator Procedure/Surgery,Active Comparator Procedure/Surger
box none&#45
TXA,Closed&#45
box IV&#45
box IA&#45
TXA,Open&#45

Sponsors

Naresuan university
Lead Sponsor
Naresuan university hospital
Collaborator

Eligibility

Sex/Gender
All
Age
20 Years to No maximum

Inclusion criteria

Inclusion criteria: All patients with the diagnosis of primary osteoarthritis knee scheduled for unilateral primary total knee arthroplasty (TKA) in Naresuan university hospital were enrolled.

Exclusion criteria

Exclusion criteria: Patients with preop hemoglobin level less than 10g/dL, previous history of thromboembolic event, renal insufficiency, cardiovascular disease or cerebrovascular accident were excluded.

Design outcomes

Primary

MeasureTime frame
Blood loss 6,12,24,48,72,96 hr postop Perioperative blood loss, drainage blood loss, postop hemoglobin level

Secondary

MeasureTime frame
pain score 6,12,24,48,72,96 hr postop visual analogue scale,knee flexion, Straight leg raising, extension lag 6,12,24,48,72,96 hr postop goniometer

Countries

Thailand

Contacts

Public ContactArtit Laoruengthana

Orthopaedic department, faculty of medicine, Naresuan university

artitlao@gmail.com+66851102799

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026