CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 12 enrolled
Drug / intervention
Powered ankle prosthesis +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02828982
NCT02828982N/ACompleted
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Determining the Potential Benefit of Powered Prostheses

Deanna H Gates·interventional·Posted Jul 12, 2016·Updated Jan 18, 2022

In Brief

A clinical study evaluating Powered ankle prosthesis and Dynamic Response Foot for Unilateral Traumatic Amputation and Amputation, Traumatic. Completed, enrolled 12 participants across 1 site.

Detailed Summary

The goal of this research is to determine the effectiveness of a powered prosthesis compared to an unpowered prosthesis during short bouts of walking, extended periods of walking (to fatigue), and performance in the community.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsUnilateral Traumatic Amputation, Amputation, Traumatic
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedJul 12, 2016
Enrollment StartJul 1, 2016
Primary CompletionAug 1, 2019
TodayJul 2, 2026
Enrollment to primary: 3.1 yearsPosted 10.0 years ago

Interventions

Powered ankle prosthesisdevice

This device is a commercially available powered ankle prosthesis, (BioM, Bionx, Bedford, MA) which was given FDA device exempt status.

Dynamic Response Footdevice

This condition is a sham condition as the participant will wear the prosthesis they were clinically prescribed and usually wear.