Can a simple blood flow cuff boost ACL recovery?
NCT ID NCT04519801
First seen Jun 24, 2026 · Last updated Jun 30, 2026 · Updated 3 times
Summary
This study tested whether adding blood flow restriction (BFR) therapy to standard physical rehabilitation helps people recover better after anterior cruciate ligament (ACL) knee surgery. Sixty active-duty military members and their families, aged 15 to 45, were randomly assigned to either standard rehab alone or standard rehab plus BFR therapy. The goal was to see if BFR therapy could improve muscle size and strength in the thigh over the course of a year.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Blood flow restriction (BFR) therapy
- What this could lead to
- If it works, this could lead to a faster, stronger recovery of leg muscle size and strength after ACL knee surgery.
- What could go wrong
- This is a small, early-stage trial with only 60 participants. The therapy may not provide significant benefits over standard rehab alone, and results may not apply to all patients.
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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60 people
The number who actually took part.
- Started
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Sep 2022
- Finished
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Mar 2026
- 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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15 to 45 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Active duty member or Department of Defense Military Health System beneficiary * 15 to 45 years of age * Indicated for ACL reconstruction with quadriceps tendon autograft with evidence of skeletal maturity; no open physes/growth plates Exclusion Criteria: * Patients undergoing a concomitant surgical procedure that would otherwise require a period of immobilization and/or restricted weight bearing (i.e. meniscal repair, meniscal allograft transplantation, osteochondral allograft transplantation, high tibial osteotomy) will be excluded. * Undergoing combined multiligamentous knee injury reconstruction * Unable to consistently participate in the prescribed post-operative rehabilitation regimen * No patients with a history of recent lower extremity deep vein thrombosis, within the 12 months or on active treatment with anticoagulants, a history of ipsilateral lower extremity lymph node dissection or a history of endothelial dysfunction. * Patients that are unable to obtain MRI secondary to either intolerance and/or implanted medical devices that preclude the safe completion of the MRI.
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Genom att skicka in godkänner du våra Användarvillkor
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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Brooke Army Medical Center- Clinical Research Center
San Antonio, Texas, 78234, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Which workout rebuilds a repaired knee best? a head-to-head trial of movement vs stability training
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- Wearable shirt tracks surgeon fatigue during knee surgery
- Vibration therapy may reduce second ACL injury risk