Bionic leg aims to restore natural walking for amputees
NCT ID NCT03204513
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a powered knee-ankle prosthetic leg in 15 people with above-knee amputations. The device uses motors to help with walking and climbing. Researchers will measure endurance, walking patterns, and quality of life to see if the bionic leg improves everyday mobility and social interaction.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Vanderbilt Powered Knee-Ankle Prosthesis (a powered prosthetic leg with motorized knee and ankle joints)
- What this could lead to
- If successful, this device could help people with above-knee amputations walk more easily and confidently in daily life.
- What could go wrong
- This is a small, early-stage trial with only 15 participants, so results may not apply to everyone. The device is complex and may not be suitable for all users.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 15 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2016
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Unilateral transfemoral level limb loss or limb difference * K2/K3/K4 level ambulators * Required to use a microprocessor knee on their prosthesis Exclusion Criteria: * Over 250 lbs body weight * Inactive, physically unfit * Cognitive deficits or visual impairment that would impair their ability to give informed consent or to follow simple instructions during the experiments * Pregnant women * Co-morbidity that interferes with the study (e.g. stroke, pace maker placement, severe ischemia cardiac disease, etc.)
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Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Shirley Ryan AbilityLab
Chicago, Illinois, 60611, United States
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