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
About this trial
This is an interventional treatment trial for Osteoathritis focused on measuring insole, osteoarthritis, pain, valgus knee
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
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
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
Learn more about this trial
Medial-Wedge Insole is Highly Effective in the Treatment of Valgus Knee Osteoarthritis
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