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Feasibility Study to Evaluate a New Energy Storage and Return Prosthetic Foot

Lower Limb Amputation Above Knee (Injury) Clinical Trial

Official title:
Prospective, Feasibility Study to Evaluate Performance, Patient Benefits, and Acceptance of a New Energy Storage and Return Prosthetic Foot

Clinical Trial Summary

A prospective, interventional, multicenter pilot study to characterize differences in performance and patient reported outcomes between the Taleo, Proflex XC, and the new Revo prosthetic foot.

Clinical Trial Description

The purpose of the Revo-M Study is to characterize differences in performance and patient reported outcomes between the Revo investigational prosthetic foot and a comparative prosthetic foot (Taleo or Proflex XC) when compared to the control foot which is the subject's currently used energy storage and return (ESR) prosthetic foot. The data obtained from this study may also serve to determine the long-term performance of Revo. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04239222
Study type Interventional
Source Otto Bock Healthcare Products GmbH
Contact
Status Completed
Phase N/A
Start date March 10, 2020
Completion date March 11, 2022
View Details
See also
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