Power knee promises smoother steps for amputees
NCT ID NCT06218238
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study compares a powered prosthetic knee (Ossur Power Knee) to a standard microprocessor knee in 20 people with above-knee amputations. Participants will use each knee for a month, then researchers measure walking speed, energy use, and sit-to-stand movements. The goal is to see if the powered knee improves mobility and whether men and women benefit differently.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Ossur Power Knee (powered prosthetic knee joint)
- What this could lead to
- If it works, this could show that a powered knee helps people with above-knee amputations walk more easily and with less effort.
- What could go wrong
- This is a small, early-stage study with only 20 participants, so results may not apply to everyone. The powered knee may not provide meaningful benefits over standard options.
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 20 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2024
- Expected to finish
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Mar 2027
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a US federal agency other than the NIH.
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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45 to 75 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 amputation (any etiology). * Age from 45-75 years. * Residual limb length classified as standard (i.e., medium) to long. * Prosthesis user for at least 1 year prior to enrolling in the study. * K3 or K4 level ambulator. * Good sensation on their residual limb(s) (upon routine clinical examination). * Good skin integrity upon visual inspection. * Does not require the use of assistive devices to walk for short distances. * Not currently taking medications that are known to affect balance or gait. * Presents with good socket fit based upon a standard assessment by the study prosthetist. Exclusion Criteria: * Bilateral amputations * Individuals with a knee disarticulation
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Jesse Brown VA Medical Center, Chicago, IL
RECRUITINGChicago, Illinois, 60612, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- New adjustable socket could help veterans walk more comfortably
- Bionic knee gets a software Tune-Up: will it help amputees walk better?