ACTRN12621001327875Not yet recruitingPhase 4
A prospective, randomised non-blinded pilot study to investigate the effect of oral tranexamic acid on the recovery time in patients undergoing primary total knee arthroplasty.
Trial Snapshot
- Phase
- Phase 4
- Status
- Not yet recruiting
- Sponsor
- Wesley Medical Research
- Enrollment
- 80
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
- Allocation
- Randomised controlled trial
- Primary Purpose
- Treatment
- Masking
- Open (masking not used)
Eligibility Criteria
- Ages
- 50 Years to o limit (—)
- Sex
- All
Inclusion Criteria
- •1. Participants of either sex scheduled to undergo a primary, unilateral Total Knee Arthroplasty.
- •2. Available for follow up at 6 months post-surgery.
- •3. Willingness to provide written, informed consent.
- •4. Willingness to comply with the study.
Exclusion Criteria
- •1. Known allergy to TXA
- •2, Acquired disturbances to colour vision
- •3, Preoperative use of anticoagulants (within 5 days of surgery)
- •4. Fibrinolytic disorders requiring intraoperative fibrinolytics
- •5. Coagulopathy, history of arteriolar or venous thromboembolic disease
- •6. Pregnancy or breastfeeding
- •7. Haemoglobin <10g/dL
Investigators
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