Personalised HTO Versus Generic HTO Virtual Clinical Trial

Completed

• Conditions: Osteoarthritis, Knee
• Interventions: Procedure: Opening wedge high tibial osteotomy; Device: Personalised subject specific custom HTO plate; Device: Generic HTO plate

• Registration Number: NCT03419598
• Lead Sponsor: University of Bath

Brief Summary

High Tibial Osteotomy (HTO) is an alternative to knee replacement in suitable patients with early knee osteoarthritis (OA), it is particularly suited to patients with single compart disease who otherwise would be suitable for unicompartmental knee replacement (UKR). OA of the knee is very common and increasing driven by the ageing of the population. The current limitations of HTO are related to the difficulty of achieving the desired correction due to a challenging surgical technique and soft tissue irritation due to the use of generic stabilisation plates. This study will examine the safety equivalence of a new patient specific HTO process which has patient specific 3D printed plates, i.e. personalised HTO plates, with the existing most commonly used HTO procedure using the Tomofix generic HTO plate. Importantly this study will be undertaken as a Virtual Trial, existing anonymised 3D imaging data will be used to create the virtual patient cohort. This cohort will receive both procedures, which for this type of procedure is only possible in a virtual scenario.

The main question to be addressed is: "Is the personalised HTO procedure as safe as the most commonly used existing generic HTO procedure?". In this context safety concerns the mechanical loads placed upon the tibia and the support plate.

The interventions will all be made on computer models, the 3D imaging data will be used to create the intact (un-operated) models of the subject tibias. Each model will then be virtually operated upon, with both the personalised and generic HTO procedures. The models will then be loaded with physiological loads experienced during function and the mechanical states compared.

Detailed Description

Ethical approval was obtained to use CT scans of 30 patients with moderate to severe knee arthritis (REC reference: 17/HRA/0033, Royal Devon \& Exeter National Health Service \[NHS\], UK).

The CT data will be used to generate the 3D geometry of each patient's proximal tibia. The osteotomy correction angle required for each patient such that the altered mechanical axis will pass through a point 62.5% of the distance from medial to lateral tibial plateau. Virtual HTO surgery will be performed on each patient to alter the mechanical axis of the knee by creating an opening wedge osteotomy.

After the virtual surgeries are performed, each virtual patient will be duplicated. One copy will have the osteotomy stabilised using a Generic plate and the other using a Personalised plate, thus forming the two arms of the trial.

For each participant in each arm finite element (FE) models will be created, and loads applied simulating walking, sit to stand and squatting. Four healings stages will be considered, stage 1 being immediately post-operation (this will not be modelled), stage 2 representing 2 weeks post-operation, stage 3 representing 6 weeks and stage 4 representing 12 weeks. The mechanical loads in the plates, and around the screw locations in the bone, will be established by solving these finite element models.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2017-01-03
• Study First Submitted: 2018-01-26
• Study First Submitted QC: 2018-01-26
• Study First Posted: 2018-02-05
• Primary Completion: 2019-06-28
• Study Completion: 2019-06-28
• Results First Submitted: 2019-10-05
• Status Verified: 2020-11
• Results First Submitted QC: 2020-11-11
• Last Update Submitted: 2020-11-11
• Results First Posted: 2020-12-07
• Last Update Posted: 2020-12-07

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• Appropriate existing CT data of lower limb.
• Male or Female, aged 18 years or above.
• Diagnosed with moderate to severe OA of the knee.

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Exclusion Criteria

• Abnormal anatomy of tibia or presence of pathology other than OA, e.g. bone tumour.
• Previous knee or osteotomy surgery.
• Presence of metal-work

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
All study participants	Generic HTO plate	All virtual participants who received a virtual opening wedge high tibial osteotomy. The baseline information was the individual CT-based geometry of tibia.
All study participants	Opening wedge high tibial osteotomy	All virtual participants who received a virtual opening wedge high tibial osteotomy. The baseline information was the individual CT-based geometry of tibia.
All study participants	Personalised subject specific custom HTO plate	All virtual participants who received a virtual opening wedge high tibial osteotomy. The baseline information was the individual CT-based geometry of tibia.

Primary Outcome Measures

Name	Time	Method
Mechanical Stress in Plate During Gait	6 weeks simulated post-operation	Mechanical stress (Von Mises) calculated for functional loading using finite element analysis

Secondary Outcome Measures

Name	Time	Method
Mechanical Strain in Bone Around Screws During Gait	6 weeks simulated post-operation	Mechanical strain calculated for functional loading using finite element analysis, note strain is dimensionless and hence has no units

Trial Locations

Locations (2)

Royal Devon & Exeter NHS Trust; 🇬🇧 Exeter, Devon, United Kingdom

University of Bath; 🇬🇧 Bath, United Kingdom