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Comparison of Different Insoles as Conservative Treatment for Medial Knee Osteoarthritis

Primary Purpose

Osteoarthritis, Knee

Status
Recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Foot deformity correcting insoles
Lateral wedge insoles
Sponsored by
Insel Gruppe AG, University Hospital Bern
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis, Knee focused on measuring Mediale Knee Osteoarthritis, Conservative Treatment, Insoles

Eligibility Criteria

40 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Informed Consent signed by the subject
  • Aged between 40 to 80 years
  • Early to mid-stage (KL 1 - 3) OA of the medial compartment of the knee based on X-ray and MRI images
  • Plano-valgus foot deformity based on clinical assessment
  • Availability of conventional radiographs, long-leg films, and a knee-MRI no older than 1 year at time of inclusion
  • Ability to walk without walking aid for more than 15min

Exclusion Criteria:

  • Contraindications and limitations of the MD as described in the instructions for use.
  • Inability to follow the procedures of the investigation, e.g. due to language problems, psychological disorders, dementia, etc. of the subject,
  • Enrolment of the PI, his/her family members, employees and other dependent persons
  • Relevant OA (Kellgren-Lawrence-Score >2) of the lateral compartment of the knee based on X-ray and MRI images
  • BMI higher than 40 kg/m
  • Fix varus deformities over 20 degrees
  • Neurological or rheumatoid diseases of any kind
  • History of high tibial osteotomy, other realignment surgery of the knee or foot
  • Foot or ankle problems that contraindicated the use of footwear load-modifying interventions
  • Relevant ligamentous instability

Sites / Locations

  • Universitätsklinik für Orthopädische Chirurgie und Traumatologie InselspitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Foot deformity correcting insole arm

Lateral wedge insole arm

Arm Description

Patients allocated to the "foot deformity correcting insole" arm will receive insoles to correct their foot deformities (plano-valgus foot deformity).

Patient allocated to the "Lateral wedge insole" arm will receive conventional lateral wedge insole.

Outcomes

Primary Outcome Measures

Numeric pain scale (NRS)
Numeric pain scale (NRS)
Numeric pain scale (NRS)
Numeric pain scale (NRS)
External knee adduction moment (EKAM)
External knee adduction moment (EKAM)
External knee adduction moment (EKAM)
External knee adduction moment (EKAM)
Knee adduction angular impulse (KAAI)
Knee adduction angular impulse (KAAI)
Knee adduction angular impulse (KAAI)
Knee adduction angular impulse (KAAI)
Western Ontario and McMaster OA Index (WOMAC)
Western Ontario and McMaster OA Index (WOMAC)
Western Ontario and McMaster OA Index (WOMAC)
Western Ontario and McMaster OA Index (WOMAC)
Western Ontario and McMaster OA Index (WOMAC)
Knee Injury and Osteoarthritis Outcome Score (KOOS)
Knee Injury and Osteoarthritis Outcome Score (KOOS)
Knee Injury and Osteoarthritis Outcome Score (KOOS)
Knee Injury and Osteoarthritis Outcome Score (KOOS)
Oxford-12 Knee Score (OKS)
Oxford-12 Knee Score (OKS)
Oxford-12 Knee Score (OKS)
Oxford-12 Knee Score (OKS)
Knee Society Score (KSS)
Knee Society Score (KSS)
Knee Society Score (KSS)
Knee Society Score (KSS)
EQ-5D
EQ-5D
EQ-5D
EQ-5D

Secondary Outcome Measures

Full Information

First Posted
July 13, 2021
Last Updated
February 8, 2023
Sponsor
Insel Gruppe AG, University Hospital Bern
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1. Study Identification

Unique Protocol Identification Number
NCT04967339
Brief Title
Comparison of Different Insoles as Conservative Treatment for Medial Knee Osteoarthritis
Official Title
A Randomized Control Trial in Patients With Medial Knee Osteoarthritis Comparing the Clinical and Biomechanical Effect of Foot Deformity Correcting Insoles and Lateral Wedge Insoles
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 1, 2021 (Actual)
Primary Completion Date
August 1, 2023 (Anticipated)
Study Completion Date
August 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Insel Gruppe AG, University Hospital Bern

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
In patients with early to mid-stage knee osteoarthritis (OA), a conservative treatment is indicated. In medial knee OA (when mainly the medial compartment of the knee is affected by OA), lateral wedge insoles have been promoted as cost effective and simple solution. However, clinical trials report conflicting results, with some reporting no benefit while others reported a small decrease in knee pain. Recent studies reported medial OA patients to have a tendency to a plano-valgus foot deformity, which is associated with a varus lower limb alignment and an internal rotation of the tibia. Some authors thus proposed the correction of plano-valgus deformity with foot deformity correcting insoles instead of lateral wedge insoles. Until today, only one study investigated the effect of foot deformity correcting insoles (e.g. with medial arch support) as alternative to lateral wedge insoles and reported encouraging results. However, they used lateral wedge insoles with custom arch support instead of foot deformity correcting customized insoles along (without lateral wedge). Furthermore, they did not perform any biomechanical analyses. The primary object of this study is to compare the effect of foot deformity correcting insoles for plano-valgus foot deformities and lateral wedge insoles on knee load distribution, knee pain and patient reported outcome measures in early to mid-stage medial knee OA patients after 6 and 12 months.
Detailed Description
Osteoarthritis (OA) of the knee is defined as an inflammatory process leading to loss of protective cartilage which results in pain, disability and loss of function. Around 25% of the population between 55 and 84 years is affected by OA of the knee. It can be graded using various classification, one of the most used being the Kellgren-Lawrence-Score (KL) ranging from 1 (early) to 4 (end stage). The treatment of choice for end-stage three compartmental knee OA (KL 4) is a total knee arthroplasty (TKA), whereby the damaged/degenerated parts of the knee are removed and replaced by a prosthesis. However, in patients with early to mid-stage OA (KL 1-3), which are usually younger patients, a conservative treatment is indicated. The goal of this conservative treatment is to relieve symptoms and at best slow progression of the diseases. In medial knee OA (when mainly the medial compartment of the knee is affected by OA), one approach is to reduce the medial compartment contact force (MCF) by shifting load from the medial (disease affected) to lateral (disease free) compartment. Thereby lateral wedge insoles have been promoted as cost effective and simple solution. The biomechanical idea of these insoles is a shift in load distribution through a change in lower limb alignment. The lateral wedge of the insoles leads to a change in foot alignment (varus hindfoot) and consequently to a change in knee alignment (valgus knee = "knock-knees") and load distribution. Biomechanical studies confirmed a reduction in external knee adduction moment (EKAM) and knee adduction angular impulse (KAAI), which are surrogate measures to estimate knee joint load distribution (e.g. MCF). However, clinical trials report conflicting results, with some reporting no benefit while others reported a small decrease in knee pain in at least some patients. In the light of this, the connection between knee OA and foot deformities has been reassessed. One study found patients with medial knee OA to have a more pronated foot type (i.e. tendency to plano-valgus deformity) compared to an age-matched control group without OA. Other investigations found more rigid foot types in patients with medial knee OA and a more internally rotated tibia during gait as well as an inversion of the forefoot. This seems important because the hindfoot axis has a significant influence on the mechanical axis of the lower limb and thereby on the load distribution in the knee. Half a degree valgisation of the hindfoot axis leads to one-degree varisation of the mechanical axis. Furthermore, a plano-valgus foot morphology was found to lead to internal rotation of the tibia which increases shear forces in the medial knee compartment. In summary, patients with medial knee OA tend to have a plano-valgus foot deformity which is associated with a varus lower limb alignment and an internal rotation of the tibia. Both have been associated to an increased loading of the medial compartment. Consequently, some authors proposed the correction of plano-valgus deformity with customized foot deformity correcting insoles instead of lateral wedge insoles as conservative treatment option for early to mid-stage medial knee OA. Until today, only one study investigated the effect of foot deformity correcting insoles (e.g. insoles with customized medial arch support) as alternative to lateral wedge insoles and reported encouraging results. However, they used lateral wedge insoles with and without medial arch support and did not explicitly only correct the foot deformity. Furthermore, they did not perform any biomechanical analysis, which seems important since some previous studies found significant differences in KAAI and EKAM among patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Knee
Keywords
Mediale Knee Osteoarthritis, Conservative Treatment, Insoles

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized control trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
25 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Foot deformity correcting insole arm
Arm Type
Experimental
Arm Description
Patients allocated to the "foot deformity correcting insole" arm will receive insoles to correct their foot deformities (plano-valgus foot deformity).
Arm Title
Lateral wedge insole arm
Arm Type
Active Comparator
Arm Description
Patient allocated to the "Lateral wedge insole" arm will receive conventional lateral wedge insole.
Intervention Type
Device
Intervention Name(s)
Foot deformity correcting insoles
Intervention Description
Foot deformity correcting insoles (e.g. insoles with medial arch support for plano-valgus deformity)
Intervention Type
Device
Intervention Name(s)
Lateral wedge insoles
Intervention Description
Lateral wedge insoles
Primary Outcome Measure Information:
Title
Numeric pain scale (NRS)
Time Frame
pre-treatment
Title
Numeric pain scale (NRS)
Time Frame
3 months
Title
Numeric pain scale (NRS)
Time Frame
6 months
Title
Numeric pain scale (NRS)
Time Frame
12 months
Title
External knee adduction moment (EKAM)
Time Frame
pre-treatment
Title
External knee adduction moment (EKAM)
Time Frame
3 months
Title
External knee adduction moment (EKAM)
Time Frame
6 months
Title
External knee adduction moment (EKAM)
Time Frame
12 months
Title
Knee adduction angular impulse (KAAI)
Time Frame
pre-treatment
Title
Knee adduction angular impulse (KAAI)
Time Frame
3 months
Title
Knee adduction angular impulse (KAAI)
Time Frame
6 months
Title
Knee adduction angular impulse (KAAI)
Time Frame
12 months
Title
Western Ontario and McMaster OA Index (WOMAC)
Time Frame
pre-treatment
Title
Western Ontario and McMaster OA Index (WOMAC)
Time Frame
3 months
Title
Western Ontario and McMaster OA Index (WOMAC)
Time Frame
6 months
Title
Western Ontario and McMaster OA Index (WOMAC)
Time Frame
9 months
Title
Western Ontario and McMaster OA Index (WOMAC)
Time Frame
12 months
Title
Knee Injury and Osteoarthritis Outcome Score (KOOS)
Time Frame
pre-treatment
Title
Knee Injury and Osteoarthritis Outcome Score (KOOS)
Time Frame
3 months
Title
Knee Injury and Osteoarthritis Outcome Score (KOOS)
Time Frame
6 months
Title
Knee Injury and Osteoarthritis Outcome Score (KOOS)
Time Frame
12 months
Title
Oxford-12 Knee Score (OKS)
Time Frame
pre-treatment
Title
Oxford-12 Knee Score (OKS)
Time Frame
3 months
Title
Oxford-12 Knee Score (OKS)
Time Frame
6 months
Title
Oxford-12 Knee Score (OKS)
Time Frame
12 months
Title
Knee Society Score (KSS)
Time Frame
pre-treatment
Title
Knee Society Score (KSS)
Time Frame
3 months
Title
Knee Society Score (KSS)
Time Frame
6 months
Title
Knee Society Score (KSS)
Time Frame
12 months
Title
EQ-5D
Time Frame
pre-treatment
Title
EQ-5D
Time Frame
3 months
Title
EQ-5D
Time Frame
6 months
Title
EQ-5D
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Informed Consent signed by the subject Aged between 40 to 80 years Early to mid-stage (KL 1 - 3) OA of the medial compartment of the knee based on X-ray and MRI images Plano-valgus foot deformity based on clinical assessment Availability of conventional radiographs, long-leg films, and a knee-MRI no older than 1 year at time of inclusion Ability to walk without walking aid for more than 15min Exclusion Criteria: Contraindications and limitations of the MD as described in the instructions for use. Inability to follow the procedures of the investigation, e.g. due to language problems, psychological disorders, dementia, etc. of the subject, Enrolment of the PI, his/her family members, employees and other dependent persons Relevant OA (Kellgren-Lawrence-Score >2) of the lateral compartment of the knee based on X-ray and MRI images BMI higher than 40 kg/m Fix varus deformities over 20 degrees Neurological or rheumatoid diseases of any kind History of high tibial osteotomy, other realignment surgery of the knee or foot Foot or ankle problems that contraindicated the use of footwear load-modifying interventions Relevant ligamentous instability
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Frank Klenke, Prof
Phone
0041 31 632 21 11
Email
ortho@insel.ch
First Name & Middle Initial & Last Name or Official Title & Degree
Andreas Hecker, MD
Phone
0041 31 632 21 11
Email
ortho@insel.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frank Klenke, Prof
Organizational Affiliation
Universitätsklinik für Orthopädische Chirurgie und Traumatologie Inselspital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Universitätsklinik für Orthopädische Chirurgie und Traumatologie Inselspital
City
Bern
ZIP/Postal Code
3010
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Andreas Andreas
Phone
004131 632 21 11

12. IPD Sharing Statement

Plan to Share IPD
No

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Comparison of Different Insoles as Conservative Treatment for Medial Knee Osteoarthritis

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