The use of compression bandages in elective orthopaedic knee surgery is well regarded, however, there is a lack of robust, well-designed evidence to support this.

The aim is to determine the feasibility of conducting a randomised control trial comparing the use of a compression bandage worn post-operatively for 24 hours after elective total knee replacement, compared to standard practice (wool and crepe, non-compressive dressing).

Inclusion Criteria:

• Age > 18
• Able to give written, informed consent
• Primary total knee replacement

Exclusion Criteria:

• Extensive peripheral vascular disease
• Lower limb neurological disorder