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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02254473
Other study ID # 1405M50501
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date August 2014
Est. completion date June 2017

Study information

Verified date February 2017
Source HealthPartners Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is looking at the efficacy of a sloped insole in patients with knee osteoarthritis. Regularly wearing a sloped insole over the course of one year will result in a wider joint space by x-ray in 60% of the subjects, a significant decrease in knee pain, decreased use of over the counter analgesics, and a clinically important improvement in the Womac pain and stiffness scale.


Recruitment information / eligibility

Status Terminated
Enrollment 12
Est. completion date June 2017
Est. primary completion date June 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 30 Years to 100 Years
Eligibility Inclusion Criteria:

- Adult patients 30 years or older with medial compartment knee Osteoarthritis (unilateral) and Grade 4 Kellgren-Lawrence39 radiographic changes presenting for treatment of knee pain.

- Range of motion knee-flexion beyond 100 degrees and not lacking more than 15 degrees of extension.

- Subtalar and forefoot motion permitting foot/ankle eversion with weight bearing.

- Sufficient shoe toe box height to allow space for the insole and therefore comfort and compliance.

- Passive laxity of medial capsule and collateral ligament by knee extension test.

Exclusion Criteria:

- All other forms of knee arthritis other than OA.

- Knee Instability- medial pseudo-opening of greater than grade 1 or detectable Anterior-posterior instability.

- Less than Grade 4 Kellgren-Lawrence radiographic changes in the medial compartment of the knee39.

- Grade 2 or greater Kellgren-Lawrence radiographic39 involvement of the patellofemoral or lateral compartment.

- Inadequate knee range of motion

- Balance problems requiring the use of a walker or wheel chair - ambulation with aid

- Diabetics with peripheral neuropathy

- Knee surgery within the past year

- Intraarticular steroid injection or visco supplementation within 6 months

- Stiff subtalar or forefoot joints - clinical test

- Inadequate shoe toe box depth to accommodate the test or control inserts

- Charcot joint

- Fixed contracture of the medial capsule and/or collateral ligament- clinical test

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Wedge Insert

Flat Insert


Locations

Country Name City State
United States TRIA Orthopaedic Center Bloomington Minnesota

Sponsors (3)

Lead Sponsor Collaborator
HealthPartners Institute Minnesota Medical Foundation, University of Minnesota - Clinical and Translational Science Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Patient Reported Function and Pain Tegner: Tegner activity level scale is a graduated list of activities of daily living, recreation, and competitive sports. The scale is 0 to 10 where 10 corresponds to normal function and 0 to unable to perform. Baseline
Primary Patient Reported Function and Pain Tegner: Tegner activity level scale is a graduated list of activities of daily living, recreation, and competitive sports. The scale is 0 to 10 where 10 corresponds to normal function and 0 to unable to perform. 6 weeks
Primary Patient Reported Function and Pain Tegner: Tegner activity level scale is a graduated list of activities of daily living, recreation, and competitive sports. The scale is 0 to 10 where 10 corresponds to normal function and 0 to unable to perform. 3 months
Primary Patient Reported Function and Pain Tegner: Tegner activity level scale is a graduated list of activities of daily living, recreation, and competitive sports. The scale is 0 to 10 where 10 corresponds to normal function and 0 to unable to perform. 6 months
Primary Patient Reported Function and Pain Tegner: Tegner activity level scale is a graduated list of activities of daily living, recreation, and competitive sports. The scale is 0 to 10 where 10 corresponds to normal function and 0 to unable to perform. 9 months
Primary Patient Reported Function and Pain Tegner: Tegner activity level scale is a graduated list of activities of daily living, recreation, and competitive sports. The scale is 0 to 10 where 10 corresponds to normal function and 0 to unable to perform. 12 months
Secondary Kellgren and Lawrence Classification of Osteoarthritis of Knee X-Ray used to measure Kellgren and Lawrence Classification of Osteoarthritis of Knee (joint space in the knee). Baseline
Secondary Kellgren and Lawrence Classification of Osteoarthritis of Knee X-Ray used to measure Kellgren and Lawrence Classification of Osteoarthritis of Knee (joint space in the knee). 6 months
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