New knee sleeve aims to cut ACL surgery pain and swelling
NCT ID NCT06240780
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether wearing Incrediwear knee products after ACL or ACL+MCL surgery helps reduce pain, swelling, and improve knee movement faster than a placebo. About 90 adults aged 18 to 65 will be randomly assigned to wear the real product, a placebo, or nothing for six months after surgery. Participants will track their pain and medication use in a daily diary.
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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 90 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2024
- 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 65 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Consented to protocol * Compliant to protocol * BMI less than 35 * Undergoing ACL or ACL+MCL within 30 days Exclusion Criteria: * Rheumatoid Arthritis * Poorly controlled diabetes (HgA1c \> 7.5) * Previous blood clots * BMI greater than 35 * Varicosities on operative leg * Pain management patient * Prior knee surgery to the operative / study knee * Worker's Comp patients * Pregnancy
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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
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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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Oklahoma Joint Reconstruction Institute
Oklahoma City, Oklahoma, 73114, United States
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Other studies related to the condition(s) this trial covers.
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