Can a 3D-Printed gadget speed up knee recovery?
NCT ID NCT06524349
First seen Aug 10, 2026 · Last updated Aug 11, 2026 · Updated 1 time
Summary
This trial explores whether using a custom 3D-printed knee extender, along with a home exercise program, helps people regain knee motion after ACL surgery. Participants who had an ACL tear will use the device at home and report their progress. The study measures how quickly they achieve full knee extension and how much swelling they have. The goal is to see if this simple tool can improve recovery outcomes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- 3D printed knee extender device used with an at-home rehabilitation program
- What this could lead to
- If it works, this could offer a low-cost, personalized tool to help people regain full knee motion faster after ACL surgery.
- What could go wrong
- This is a small early-stage study, and results may not apply to everyone. The device is new, and its benefits over standard rehab are not yet proven.
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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45 people
The number who actually took part.
- Started
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Jun 2024
- Finished
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Dec 2025
- 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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14 to 60 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: * Diagnosed with a primary ACL rupture. Secondary knee pathology such as, but not limited to bone edema, strains, and meniscal pathology are acceptable as long as the primary injury and indication for surgery is the ACL rupture. * Able and willing to adhere to the study procedures * Able to consent for self-, or able to assent for self with parental consent Exclusion Criteria: * Pregnancy * Non-English speaking
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Conditions
The condition(s) this trial relates to.
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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Sanford Orthopedics and Sports Medicine
Fargo, North Dakota, 58103, United States
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Sanford Orthopedics and Sports Medicine
Sioux Falls, South Dakota, 57104, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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