ISRCTN87127065CompletedPhase 3
A randomised controlled trial of the effect of a two-layer compression bandage system on knee function following total knee arthroplasty
orthumbria Healthcare NHS Foundation Trust0 sites2,338 target enrollmentStarted: February 20, 2017Last updated:
Conditions
Trial Snapshot
- Phase
- Phase 3
- Status
- Completed
- Sponsor
- Enrollment
- 2,338
Study Overview
Brief Summary
2019 Protocol article in https://www.ncbi.nlm.nih.gov/pubmed/31068223 protocol (added 10/05/2019) 2020 Other publications in https://pubmed.ncbi.nlm.nih.gov/35600143/ An embedded randomised controlled retention trial of personalised text messages compared to non-personalised text messages in an orthopaedic setting (added 31/10/2022)
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Sex
- All
Inclusion Criteria
- •1. Patients scheduled for primary total knee arthroplasty
- •2. Presenting at a participating trial site
- •3. Aged over 18
- •4. Able to provide written informed consent
Exclusion Criteria
- •1. Unable to consent
- •2. History of peripheral vascular disease
- •3. History of peripheral neuropathy
- •4. History of, or current venous ulceration
- •5. Absent foot pulses
- •6. Planned same day discharge joint replacement patients
- •7. Revision knee arthroplasty
- •8. Unicondylar or patellofemoral joint knee arthroplasty
- •9. Regular concomitant high dose anti-coagulant medication. Patients on routine thromboprophylaxis can be included
- •10. Unwilling to provide informed consent
- •11. Lack mental capacity and therefore unlikely to comply with data collection
Investigators
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