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Clinical Trial Summary

The purpose of this study is to develop criteria for prosthetic foot prescription for Veterans and Service Members with transtibial limb loss. The objectives are to: 1) Determine the appropriate functional outcome tests and measures to support the prescription of a type of Energy Storing and Returning (ESR) non-articulating, articulating or active plantarflexion prosthetic ankle-foot for a Veteran or Service Member with transtibial limb loss. 2) Correlate patient goals and subjective measures with objective data to determine the appropriate prosthetic ankle-foot category that will facilitate the greatest overall function to the user. 3) Develop criteria for the appropriate prescription of non-articulating ESR, articulating ESR, and active plantar flexion ESR ankle-foot units.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03505983
Study type Interventional
Source VA New York Harbor Healthcare System
Contact
Status Active, not recruiting
Phase N/A
Start date August 1, 2017
Completion date December 31, 2024

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