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Clinical Trial Summary

This study will assess if the functional performance and musculoskeletal outcome of transfemoral amputees are improved after receiving a Microprocessor Knee (MPK) compared to a Non-Microprocessor Knees (NMPK).


Clinical Trial Description

The study design is a reversal design whereby only the prosthetic knee joint will be changed. Each subject will be tested using their current NMPK, fit and tested with a MPK, and then tested again with their NMPK. MPK prostheses from all manufacturers will be considered appropriate for testing. Each MPK to be used in this study is FDA approved. The foot will be in the L5981 class, e.g. flex foot or equivalent. The same socket, suspension, and foot will be used throughout the study in order to eliminate these confounding variables. All prosthesis fittings will be performed by the subject's own certified prosthetist according to manufacturers' fitting guidelines. ;


Study Design


Related Conditions & MeSH terms

  • Lower Limb Amputation Above Knee (Injury)

NCT number NCT02240186
Study type Interventional
Source Mayo Clinic
Contact
Status Completed
Phase N/A
Start date June 2014
Completion date December 2017

See also
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