Knee Replacement Bandaging Study (KReBS)
Research type
Research Study
Full title
A Randomised Controlled Trial of the effect of a Two-layer Compression Bandage System on Knee Function following total knee arthroplasty
IRAS ID
212212
Contact name
Mike Reed
Contact email
Sponsor organisation
Northumbria Healthcare NHS Foundation Trust
Duration of Study in the UK
2 years, 0 months, 1 days
Research summary
The use of compression bandages in elective orthopaedic knee surgery is well regarded, however, there is a lack of robust, well-designed trials to support this.
The aim is to conduct a randomised controlled trial comparing the use of a two-layer compression bandage worn post-operatively for up to 48 hours after elective total knee replacement, compared to standard practice (non-compressive bandaging).
The study aims to test the hypothesis that the use of a two-layer Compression Bandage System improves function compared to standard wool and crepe bandage, following total knee replacement.
Patients will be approached to take part from participating hospitals and those who agree to be included in this trial will be allocated at random to either of the two treatments.
Outcome will be assessed using a patient self-reported questionnaire which measures knee pain and function after one year.
The associated costs of both treatments to the NHS will also be evaluated.
REC name
North East - Newcastle & North Tyneside 2 Research Ethics Committee
REC reference
16/NE/0400
Date of REC Opinion
1 Feb 2017
REC opinion
Further Information Favourable Opinion