Clinical Trials Directory

Trials / Completed

CompletedNCT00076453

A Study of Orthotic Shoe Inserts for Controlling Osteoarthritic Knee Pain

Clinical Effects of Altered Biomechanics in Knee Osteoarthritis

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Rush University Medical Center · Academic / Other
Sex
All
Age
25 Years
Healthy volunteers
Accepted

Summary

Osteoarthritis is a degenerative joint disease and is the most common form of arthritis. This study will evaluate the effectiveness of customized shoe inserts in controlling and relieving the pain of knee osteoarthritis.

Detailed description

Osteoarthritis (OA) is a chronic disease causing deterioration of the joint cartilage and the formation of bone spurs at the margins of the joints. Knee OA causes substantial pain, suffering, and disability, as well as enormous economic burden on the patient; unfortunately, treatment provides relief but not a cure. The majority of patients with symptomatic knee OA do not attain satisfactory long-term relief, even with recent advances in pain relievers. Analgesic treatment may relieve the pain but does not improve biomechanics and may even aggravate OA. Although OA is complex and not completely understood, disease onset and progression are at least partly related to responses by bone and cartilage to biomechanical loading. Devices that promote pressure reduction from the medial knee may provide pain relief while simultaneously protecting the joint from further degeneration; one such device is a lateral wedge orthotic shoe insert. When worn during weight-bearing activity, these inserts have been shown to reduce loading of the medial compartment and may provide pain relief. This study will evaluate the effectiveness of orthotic shoe inserts in controlling and relieving knee OA. The study will also assess improvements in loading biomechanics of the knee. This is a 3-year study. Patients will be randomly assigned to one of two groups; the first group will receive lateral wedge orthotic inserts and the second group will receive standard orthotic inserts. There will be 10 study visits during the course of the study. Patients will undergo X-rays and bone mineral density testing (DEXA) and 3 blood collections during the course of the study.

Conditions

Interventions

TypeNameDescription
DEVICELateral wedge orthotic shoe insertsCustomized lateral wedge orthotic shoe inserts
DEVICEStandard orthotic shoe insertsNeutral orthotic inserts

Timeline

Start date
2003-06-01
Primary completion
2007-12-01
Completion
2007-12-01
First posted
2004-01-26
Last updated
2011-09-27

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00076453. Inclusion in this directory is not an endorsement.