Bionic knee gets a software Tune-Up: will it help amputees walk better?
NCT ID NCT06620861
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested a new firmware (software) update for the Power Knee, a bionic knee used by people who have lost a leg above the knee. Six participants tried both the new and current firmware while doing daily tasks like standing up, walking, and climbing stairs. The goal was to see if the update made these activities easier. The study was terminated early, so results are limited.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Power Knee firmware update (device software)
- What this could lead to
- If successful, this firmware update could improve how well the Power Knee helps with everyday movements like standing up, walking, and climbing stairs.
- What could go wrong
- This was a very small, early study (only 6 participants) that was terminated early, so results are limited and may not apply to all users. The update may not offer noticeable benefits.
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
-
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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6 people
The number who actually took part.
- Started
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Dec 2024
- Finished
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Dec 2024
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
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 years and older
- 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: * 50 kg \< body weight \< 116 kg * lower limb loss, amputation or deficiency * cognitive ability to understand all instructions and questionnaires in the study * Unilateral transfemoral amputees that are regular Power Knee users for at least 4 weeks * age ≥ 18 years * Moderate to high active subjects * Willing and able to participate in the study and follow the protocol * Comfortable and stable socket fit * No socket issues/changes in the last 6 weeks Exclusion Criteria: * Users with pain * Bilateral amputees * Users using passive microprocessor controlled knees * Users with cognitive impairment * Users with co-morbidities in the contra lateral limb, which affect their functional mobility * Hip disarticulation amputees * Users with osseointegrated prosthesis * Pregnant users
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Oakland Orthopedic Appliances Inc
Bay City, Michigan, 48708, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- How does losing more of a leg change strength and balance? researchers measure the difference
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- Can bionic limbs feel real? a trial tests touch feedback for amputees
- Can a common anesthetic dampen phantom limb pain?
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