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Medial-Wedge Insole is Highly Effective in the Treatment of Valgus Knee Osteoarthritis

Primary Purpose

Osteoathritis

Status
Terminated
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Medial-Wedge Insole intervention
Sponsored by
University of Sao Paulo
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoathritis focused on measuring insole, osteoarthritis, pain, valgus knee

Eligibility Criteria

45 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • knee osteoarthritis with bilateral valgus deformity greater than or equal to 8°.
  • Radiographic grading of OA was defined according to Kellgren and Lawrence (KL)class II or more
  • pain on movement > 2 measured by Visual Analog Scale (VAS).

Exclusion Criteria:

  • body mass index (BMI) > 40
  • scoliosis
  • lower limbs length difference exceeding 1 cm
  • knee surgery
  • hallux rigidus
  • previous history of rheumatologic disease (rheumatoid arthritis, connective tissue disease, microcrystalline arthropathy,soronegative arthropathy)
  • soft tissue involvement (anserine, patellar, and calcaneal tendinopathy)
  • foot/lower leg symptoms

Sites / Locations

    Outcomes

    Primary Outcome Measures

    To assess symptoms, Visual Analog Scale (VAS) will be used for night pain, pain at rest and on movement. Lequesne index score and the WOMAC questionnaire will be applied at baseline and after 8 weeks by a blinded examiner.

    Secondary Outcome Measures

    Antero-posterior conventional X-ray of knees and ankles were both performed under monopodalic load with and without insoles in order to measure femorotibial, talocalcaneal, and talus tilt angles.

    Full Information

    First Posted
    April 27, 2007
    Last Updated
    April 27, 2007
    Sponsor
    University of Sao Paulo
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00467337
    Brief Title
    Medial-Wedge Insole is Highly Effective in the Treatment of Valgus Knee Osteoarthritis
    Official Title
    Medial-Wedge Insole is Highly Effective in the Treatment of Valgus Knee Osteoarthritis
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2007
    Overall Recruitment Status
    Terminated
    Why Stopped
    Terminated
    Study Start Date
    June 2004 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    June 2006 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    University of Sao Paulo

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    To assess the efficacy of medial-wedge insole in valgus knee osteoarthritis (OA). We hypothesized that medial-wedged insoles are biomechanically effective and should reduce lateral compartment loading in persons with valgus knee osteoarthritis with a consequent symptomatic improvement.
    Detailed Description
    Thirty females fulfilling the American College of Rheumatology criteria for knee osteoarthritis with bilateral valgus deformity greater than or equal to 8° were consecutively will be selected from the Rheumatology Outpatient Clinic of University of São Paulo. Radiographic grading of OA was defined according to Kellgren and Lawrence (KL) and analyzed blind by the same rheumatologist. Inclusion criteria were knee osteoarthritis with lateral compartment involvement detected on X-Ray (KL class II or more); absence or minimal (KL class 0 or I) for medial compartment involvement; and pain on movement > 2 measured by Visual Analog Scale (VAS). Exclusion criteria were: body mass index (BMI) > 40, scoliosis, lower limbs length difference exceeding 1 cm, knee surgery, hallux rigidus, previous history of rheumatologic disease (rheumatoid arthritis, connective tissue disease, microcrystalline arthropathy, and soronegative arthropathy), soft tissue involvement (anserine, patellar, and calcaneal tendinopathy), and foot/lower leg symptoms. Corticosteroid and hyaluronic acid infiltrations were not allowed 3 and 6 months prior to entry, respectively. The use of non-steroidal anti-inflammatory and analgesics or slow action drugs (DMARDs) were allowed if prescribed at least four weeks and eight weeks before entry and remained unchanged throughout the study. The study was approved by the local Ethical Committee and all patients signed informed consent. Study protocol: Patients will be randomly assigned into 2 groups: CASES with 16 patients and CONTROLS with fourteen patients. The CASES wore 8 mm high, medial-wedged insoles for the hind foot inserted into a new shoe for 8 weeks. The CONTROLS will use an insole resembling the former group, only without raised wedges (FIGURE 1-B) for 8 weeks. Patients of both groups will receive the same new shoe and were blind to the insole use. The ethylene-vinyl-acetate (EVA - density 50) insoles were provided by the AACD Institute (Handicapped Child Care Association). A commercial neoprene with elastic banding will be used for ankle support. Both groups will use similar standard shoes supplied by the hospital. Each participant will be instructed to use the splints (shoes and elastic banding) for 3 to 6 hours daily. The correct use of the splints will be checked every two weeks. Undesirable side-effects will be recorded at the end of the study. Age, disease duration, weight, height, body mass index (BMI), and sedentarism (only daily activities) will be recorded for all patients at entry. In order to assess symptoms, Visual Analog Scale (VAS) will be used for night pain, pain at rest and on movement. Lequesne index score and the WOMAC questionnaire will be applied at baseline and after 8 weeks by a blinded examiner. Antero-posterior conventional X-ray of knees and ankles will be performed under monopodalic load with and without insoles in order to measure femorotibial, talocalcaneal, and talus tilt angles. Femorotibial angle is formed by the intersection of femur and tibia axes, obtained through lines drawn at distal one-third of the femur and proximal one-third of the tibia, both equidistant from external limits of the cortical bones. Talocalcaneal angle is formed by a first line connecting the midpoints between the trochanter talus to the lateral and medial malleoli, and a second line perpendicular to the floor identified by inferior border of X-ray. Tilt angle of talus is formed by a line parallel to floor and the tilt of the trochanter talus. All angles will be measured blind by the same rheumatologist.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Osteoathritis
    Keywords
    insole, osteoarthritis, pain, valgus knee

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    Double
    Allocation
    Randomized

    8. Arms, Groups, and Interventions

    Intervention Type
    Procedure
    Intervention Name(s)
    Medial-Wedge Insole intervention
    Primary Outcome Measure Information:
    Title
    To assess symptoms, Visual Analog Scale (VAS) will be used for night pain, pain at rest and on movement. Lequesne index score and the WOMAC questionnaire will be applied at baseline and after 8 weeks by a blinded examiner.
    Time Frame
    2 years
    Secondary Outcome Measure Information:
    Title
    Antero-posterior conventional X-ray of knees and ankles were both performed under monopodalic load with and without insoles in order to measure femorotibial, talocalcaneal, and talus tilt angles.
    Time Frame
    2 years

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    45 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: knee osteoarthritis with bilateral valgus deformity greater than or equal to 8°. Radiographic grading of OA was defined according to Kellgren and Lawrence (KL)class II or more pain on movement > 2 measured by Visual Analog Scale (VAS). Exclusion Criteria: body mass index (BMI) > 40 scoliosis lower limbs length difference exceeding 1 cm knee surgery hallux rigidus previous history of rheumatologic disease (rheumatoid arthritis, connective tissue disease, microcrystalline arthropathy,soronegative arthropathy) soft tissue involvement (anserine, patellar, and calcaneal tendinopathy) foot/lower leg symptoms
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Ricardo Fuller, MD PhD
    Organizational Affiliation
    Rheumatology Division HCFMUSP
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Eloisa Bonfa, MD PhD
    Organizational Affiliation
    Rheumatology Division HCFMUSP
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    18438931
    Citation
    Rodrigues PT, Ferreira AF, Pereira RM, Bonfa E, Borba EF, Fuller R. Effectiveness of medial-wedge insole treatment for valgus knee osteoarthritis. Arthritis Rheum. 2008 May 15;59(5):603-8. doi: 10.1002/art.23560.
    Results Reference
    derived

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    Medial-Wedge Insole is Highly Effective in the Treatment of Valgus Knee Osteoarthritis

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