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Effect of Tranexamic acid in reducing the bleeding of knee replacement

Comparison of intravenous injection of tranexamic acid before and at the end of surgery with no injection of the drug to control bleeding after total knee arthroplasty (TKA).

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200526047574N1
Enrollment
153
Registered
2020-06-17
Start date
2020-06-07
Completion date
Unknown
Last updated
2020-07-13

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

Conditions

knee replacement. Osteoarthritis of knee

Interventions

Intervention 1: Intervention group 1: 2 ampoules of 500 mg tranexamic acid, intravenously, One dose, One hour before surgery. Intervention 2: Intervention group 2: 2 ampoules of 500 mg tranexamic aci

Sponsors

Dr. Ali Shariati Hospital/ Orthopedic ward
Lead Sponsor

Eligibility

Sex/Gender
All
Age
53 Years to 84 Years

Inclusion criteria

Inclusion criteria: 1)Patients need total knee replacement 2)Patients have no coagulation problems 3)Patients have no underlying disease 4)Patients have no history of thrombophlebitis 5)Patients compliance to participate in the study

Exclusion criteria

Exclusion criteria: 1)Patients have coagulation problem 2)Patients have history of thrombophlebitis 3)Patients have history of cardiovascular and brain disease 4)Patients non compliance to participate in the study 5)Pregnancy

Design outcomes

Primary

MeasureTime frame
The amount of blood collected inside the drains after surgery. Timepoint: 24 hours after surgery. Method of measurement: Measuring the amount of blood collected inside the drains in cm3 (cc).

Secondary

MeasureTime frame
Observation the size of knee hemarthrosis after surgery. Timepoint: 48 hours after surgery. Method of measurement: Observation and examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAnis Salimi

School of medicine/Islamic Azad University, Najafabad Branch

anis.salimi2013@gmail.com+98 31 3777 3623

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026