Bespoke vs Standard Instrumentation in TKR

  • Research type

    Research Study

  • Full title

    Randomised controlled trial of patient-specific instrumentation vs standard instrumentation in total knee arthroplasty

  • IRAS ID

    166681

  • Contact name

    Leela Biant

  • Contact email

    leela.biant@manchester.ac.uk

  • Sponsor organisation

    Research and Development Department

  • Duration of Study in the UK

    4 years, 0 months, 1 days

  • Research summary

    Total knee replacement (TKR) is an established treatment for knee osteoarthritis and leads to a satisfactory outcome in over 75% of patients. The pain and function after TKR can be dependent on the accuracy of initial implantation, as deviation of more than 3 degrees from the normal alignment of the limb can lead to abnormal stresses on the implant and accelerated failure. Patient specific cutting blocks may result in a more individualised implant placement, improved pain and function following surgery, and a longer-lasting implant.
    This trial is designed to investigate if there is any benefit to bespoke instrumentation in terms of pain and function to the patient, and an economic benefit to the NHS.

  • REC name

    South East Scotland REC 01

  • REC reference

    15/SS/0024

  • Date of REC Opinion

    16 Feb 2015

  • REC opinion

    Unfavourable Opinion