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Intra-articular VS Intravenous Tranexamic Acid in Total Knee Arthroplasty

Intra-articular VS Intravenous Tranexamic Acid in Total Knee Arthroplasty - A Randomized Controlled Trial Comparing Effectiveness and Safety

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004440
Enrollment
Unknown
Registered
2014-03-29
Start date
2014-03-28
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Knee Osteoarthritis

Interventions

Two groups:To compare the blood-saving effects and risks of developing symptomatic thromboembolic events after total knee arthroplasty by using intra-articular and intravenous tranexamic acid

Sponsors

Dr KY Chung
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusive criteria are subjects with degenerative osteoarthritis of knee joints, who are scheduled for TKA with posterior stabilized total knee prosthesis.

Exclusion criteria

Exclusion criteria: Exclusion criteria are patients with pre-operative anemia with haemoglobin level less than 12 g/dL (reference of PWH lab), known allergy to TNA, deep vein thrombosis, pulmonary embolism, ischemic stroke, those on anticoagulant drugs including warfarin and Plavix, or those undergo TKA under epidural anesthesia, those with renal impairment(with creatinine level >200) and inflammatory arthritic patient.

Design outcomes

Primary

MeasureTime frame
Blood loss after operation, based on the change in haemoglobin level, drain output and wound discharge at baseline and post-operation day 5;any symptomatic thromboembolic events after operation at post-operation day 5;

Secondary

MeasureTime frame
Length of stay in hospital;

Countries

China

Contacts

Public ContactDr KY Chung
kychung@ort.cuhk.edu.hk+852 26321819

Outcome results

None listed

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