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Bespoke vs Standard Instrumentation in TKR

Primary Purpose

Knee Osteoarthritis

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Patient specific cutting blocks
Conventional cutting blocks
Sponsored by
NHS Lothian
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Knee Osteoarthritis focused on measuring Total Knee Replacement, Patient Specific Instrumentation

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with osteoarthritis ('wear and tear') of the knee which is sufficiently symptomatic to require knee arthroplasty as assessed by their consultant orthopaedic surgeon

Exclusion Criteria:

  • Patients with inflammatory arthropathy, patients requiring bone augmentation, ligament incompetence, values deformity > 5 degrees

Sites / Locations

  • Royal Infirmary of EdinburghRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Patient Specific Cutting Blocks

Conventional Cutting Blocks

Arm Description

For the bespoke individualised cutting blocks to be manufactured, the patients will undergo a preoperative CT scan under a set protocol. The CT radiation dose will be considerably less than a conventional diagnostic CT scan.

The patients in this arm will be operated on using conventional instruments.

Outcomes

Primary Outcome Measures

Limb alignment
Measured in degrees from Hip-Knee-Ankle radiographs from centre of femoral head to midpoint of the ankle

Secondary Outcome Measures

Difference between baseline pre-op and one year post-op change in gait measured using a bespoke clinic-appropriate motion analysis system.
Knee range of motion, strength and gait analysis assessments will be carried out on a bespoke clinic-appropriate motion analysis system. This system consists of 8 Vicon B10 Bonita cameras (Vicon Systems, Oxford) which immediately surround a self-paced N-Mill treadmill (Motekforce Link, Amsterdam).
Difference in patient reported knee pain level as measured by Oxford Knee Score between baseline and one year and also between study groups.
Validated patient reported knee pain questionnaires as measured by Oxford Knee Score (out of 48 points) pre-operation and at one year post-operation. Difference between baseline and one year scores for each patient and also analysed between groups (patient specific cutting blocks compared to conventional cutting blocks).
Difference in patient reported knee function between baseline and one year and also between study groups.
Validated patient reported knee function questionnaires as measured by EQ-5D pre-operation and at one year post-operation. Difference between baseline and one year scores for each patient and also analysed between groups (patient specific cutting blocks compared to conventional cutting blocks).
Difference in patient reported quality of life questionnaires between baseline and one year and also between study groups.
Validated quality of life questionnaires as measured by SF-12 score pre-operation and at one year post-operation. Difference between baseline and one year scores for each patient and also analysed between groups (patient specific cutting blocks compared to conventional cutting blocks).
Healthcare cost
Healthcare cost measured in pounds sterling (GBP). Total cost of performing knee replacement using conventional cutting blocks compared to using bespoke cutting blocks and disposable instrumentation. The measurable contributors to the costs of healthcare include operating time (minutes), number of instrument trays requiring sterilisation (number of trays), length of hospital stay (days), patient transfusion requirement (number of units of packed cells required), cost of bespoke disposable instrumentation (GBP).

Full Information

First Posted
March 21, 2016
Last Updated
July 22, 2016
Sponsor
NHS Lothian
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1. Study Identification

Unique Protocol Identification Number
NCT02845206
Brief Title
Bespoke vs Standard Instrumentation in TKR
Official Title
Randomised Controlled Trial of Patient Specific Instrumentation vs Standard Instrumentation in Total Knee Arthroplasty
Study Type
Interventional

2. Study Status

Record Verification Date
February 2016
Overall Recruitment Status
Unknown status
Study Start Date
February 2016 (undefined)
Primary Completion Date
February 2018 (Anticipated)
Study Completion Date
February 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
NHS Lothian

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief 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 long-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.
Detailed Description
Total knee replacement (TKR) is an established treatment for 'wear and tear' arthritis and leads to a satisfactory outcome in over 75% of patients. However, this means that up to 25% of patients are not entirely satisfied with their TKR. The longevity and stability of a TKR is greatly dependent on the accuracy of the initial surgery. Deviation of more than 3 degrees from the normal axis can lead to abnormal stresses causing the implants to fail. 'Patient specific' technology involves preoperative computer assessment of the patients' knee and allows for a 'patient specific' cutting block to be manufactured. This will allow for individual bony cuts specific to the patients own anatomy. 'Patient specific' implants and cutting blocks may allow a more optimal implant positioning and are implanted without the need for instrumentation of the femoral medullary canal (thigh), so lower blood loss may result. This could result in improved early range of movement and decreased pain following surgery. The total knee replacement used in this study will be the GMKSphere (Medacta International) TKR. It has a specific design which more closely resembles a natural unreplaced knee than any other knee replacement. It may help address the phenomenon of 'mid flexion instability', which is where the patient perceives their replaced knee to be unsteady on stairs and slopes. Patient specific technology may also result in a cost saving, as it potentially reduces the number of sterilised trays required during the surgery. This study will allow for comparison in knee function and patient outcomes between patients who have undergone their TKR with patient specific cutting blocks compared to conventional cutting blocks. The scans obtained following the surgery could lead to world leading methodology for the assessment of knee replacements and would set a blue print for the evaluation of other knee implants in the future.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Osteoarthritis
Keywords
Total Knee Replacement, Patient Specific Instrumentation

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
172 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Patient Specific Cutting Blocks
Arm Type
Experimental
Arm Description
For the bespoke individualised cutting blocks to be manufactured, the patients will undergo a preoperative CT scan under a set protocol. The CT radiation dose will be considerably less than a conventional diagnostic CT scan.
Arm Title
Conventional Cutting Blocks
Arm Type
Active Comparator
Arm Description
The patients in this arm will be operated on using conventional instruments.
Intervention Type
Procedure
Intervention Name(s)
Patient specific cutting blocks
Intervention Description
'MyKnee' Instrumentation
Intervention Type
Procedure
Intervention Name(s)
Conventional cutting blocks
Intervention Description
Standard Instrumentation
Primary Outcome Measure Information:
Title
Limb alignment
Description
Measured in degrees from Hip-Knee-Ankle radiographs from centre of femoral head to midpoint of the ankle
Time Frame
1 years
Secondary Outcome Measure Information:
Title
Difference between baseline pre-op and one year post-op change in gait measured using a bespoke clinic-appropriate motion analysis system.
Description
Knee range of motion, strength and gait analysis assessments will be carried out on a bespoke clinic-appropriate motion analysis system. This system consists of 8 Vicon B10 Bonita cameras (Vicon Systems, Oxford) which immediately surround a self-paced N-Mill treadmill (Motekforce Link, Amsterdam).
Time Frame
1 year
Title
Difference in patient reported knee pain level as measured by Oxford Knee Score between baseline and one year and also between study groups.
Description
Validated patient reported knee pain questionnaires as measured by Oxford Knee Score (out of 48 points) pre-operation and at one year post-operation. Difference between baseline and one year scores for each patient and also analysed between groups (patient specific cutting blocks compared to conventional cutting blocks).
Time Frame
1 year
Title
Difference in patient reported knee function between baseline and one year and also between study groups.
Description
Validated patient reported knee function questionnaires as measured by EQ-5D pre-operation and at one year post-operation. Difference between baseline and one year scores for each patient and also analysed between groups (patient specific cutting blocks compared to conventional cutting blocks).
Time Frame
1 year
Title
Difference in patient reported quality of life questionnaires between baseline and one year and also between study groups.
Description
Validated quality of life questionnaires as measured by SF-12 score pre-operation and at one year post-operation. Difference between baseline and one year scores for each patient and also analysed between groups (patient specific cutting blocks compared to conventional cutting blocks).
Time Frame
1 year
Title
Healthcare cost
Description
Healthcare cost measured in pounds sterling (GBP). Total cost of performing knee replacement using conventional cutting blocks compared to using bespoke cutting blocks and disposable instrumentation. The measurable contributors to the costs of healthcare include operating time (minutes), number of instrument trays requiring sterilisation (number of trays), length of hospital stay (days), patient transfusion requirement (number of units of packed cells required), cost of bespoke disposable instrumentation (GBP).
Time Frame
1 year

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with osteoarthritis ('wear and tear') of the knee which is sufficiently symptomatic to require knee arthroplasty as assessed by their consultant orthopaedic surgeon Exclusion Criteria: Patients with inflammatory arthropathy, patients requiring bone augmentation, ligament incompetence, values deformity > 5 degrees
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Susan Shepherd
Email
susan.shepherd@nhslothian.scot.nhs.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Douglas Young
Email
douglas.young@nhslothian.scot.nhs.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Leela C Biant, FRCSEd(Tr&Orth) MSres MFSTEd
Organizational Affiliation
University of Edinburgh
Official's Role
Principal Investigator
Facility Information:
Facility Name
Royal Infirmary of Edinburgh
City
Edinburgh
State/Province
Lothian
ZIP/Postal Code
EH16 4SA
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
Phone
0131 536 1000

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Data available to bone fide researchers at the end of the study

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Bespoke vs Standard Instrumentation in TKR

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