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Clinical Trial Summary

This study will examine clinical outcomes related to pain and function in patients with anterior knee pain (i.e. focal patella and/or trochlea cartilage defect(s), patellofemoral arthritis) before and after standard of care, non-surgical management with and without the addition of a Tri-Compartment Unloader (TCU) knee brace during activities of daily living. Randomly selected participants will wear a TCU brace for several weeks during physical therapy and activities of daily living that is designed to reduce compressive forces in all three compartments of the knee during weight-bearing flexion. Our hypothesis is that TCU bracing will improve clinical outcomes relatednto pain and function.


Clinical Trial Description

Patients in this study have been identified as good candidates by their physicians. As the study procedures closely follow the standard of care procedures in place, study participation presents little additional risk above and beyond the standard of care procedures. The study was designed to present the least risk possible consistent with sound research design. Participants in this study will undergo standard of care X-rays that will help in eligibility determination. Participants will be randomized to either group, and will have a 50% chance of receiving the brace. Outcomes will be measured at baseline (before any intervention), 6 weeks after commencing rehabilitation at Stanford, and 3 months after commencing rehabilitation at Stanford. These outcome measures are collected using PatientiQ which is is being used at the clinic as part of standard of care. Spring Loaded Tech is providing the TCU braces for the patients in this study at no cost. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05428332
Study type Interventional
Source Stanford University
Contact Monica S Vel, BS
Phone (650) 721-7653
Email msvel@stanford.edu
Status Recruiting
Phase N/A
Start date April 5, 2022
Completion date December 5, 2024

See also
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Recruiting NCT02786784 - The Role of Arthrogenic Muscular Inhibition in Patellofemoral Pain and the Response to an Exercise Programme N/A
Completed NCT02914574 - The Patellofemoral Pain Functional Performance Study N/A
Completed NCT05367375 - Comparison of Removing and Non-removing Patellofemoral Joint Osteophytes Following Medial Unicompartment Knee Arthroplasty
Recruiting NCT06398535 - Ultrasound Versus Magnetic Reseonance Imaging(MRI) in the Assessment of Anterior Knee Pain