New knee brace aims to ease pain after ACL surgery
NCT ID NCT07090616
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compares a new knee brace called KRONOS to the standard Breg T-Scope brace after ACL reconstruction surgery. Researchers want to see if the KRONOS brace reduces pain and helps people recover knee motion faster. About 40 adults having ACL surgery will be randomly assigned to one of the two braces.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- knee brace (device)
- What this could lead to
- If it works, this could point toward a more comfortable and effective brace for ACL recovery, reducing pain and improving knee motion.
- What could go wrong
- This is a small, early-stage trial with only 40 participants, so results may not apply to everyone. The new brace may not be significantly better than the standard one.
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 40 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2025
- Expected to finish
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Jan 2028
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 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: * Subjects \> 18 years of age * English-speaking * Scheduled to undergo primary anterior cruciate ligament reconstruction surgery * No history of prior knee surgery on the operative knee * No concomitant ligamentous repair or reconstruction procedures (i.e. ligamentous pathology aside from anterior cruciate ligament). * Subjects undergoing concurrent partial meniscectomy or meniscus repair that would not alter postoperative weight-bearing status or rehabilitation protocol would be eligible for inclusion. * Clinical and radiographic examination (MRI) consistent with an acute full thickness ACL tear Exclusion Criteria: * Age \< 18 years of age * Non-English speaking * Revision ACL reconstruction * Multi-ligamentous injury, including concomitant posterior cruciate ligament, medial collateral ligament and fibular collateral ligament injuries * Concomitant meniscal or cartilage injury that would alter postoperative weight bearing status or rehabilitation protocol * Inability to comply with the proposed follow-up clinic visits * Subjects lacking decisional capacity * Worker's compensation subjects * Requiring a custom-sized brace
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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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Rush University Medical Center
RECRUITINGChicago, Illinois, 60612, United States
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