ACTRN12621001327875
Not yet recruiting
Phase 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.
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Wesley Medical Research
- Enrollment
- 80
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
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
Outcomes
Primary Outcomes
Not specified
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