Can a cuff boost ACL recovery? new study tests blood flow restriction
NCT ID NCT07406763
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether adding blood flow restriction (BFR) to standard rehab exercises helps people recover better after anterior cruciate ligament (ACL) reconstruction. 36 adults aged 18-35 were randomly assigned to either standard rehab or standard rehab plus BFR. Researchers measured muscle strength, knee position sense, range of motion, pain, and function before surgery and at 1.5 and 3 months after. The goal was to see if BFR could 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
- Blood flow restriction device
- What this could lead to
- If it works, this could lead to a more effective rehab program for people recovering from ACL surgery, helping them regain strength and function faster.
- What could go wrong
- This is a small, early-stage trial with only 36 participants. Results may not apply to everyone, and the benefits of blood flow restriction might be modest or not last long.
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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36 people
The number who actually took part.
- Started
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Feb 2020
- Finished
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Feb 2022
- 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 35 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 Male or female participants aged 18-35 years Undergoing primary unilateral anterior cruciate ligament reconstruction Reconstruction performed using semitendinosus tendon autograft Referred for postoperative rehabilitation by an orthopedic surgeon Medically cleared to participate in postoperative rehabilitation and exercise training Ability to understand and follow verbal instructions Willingness to participate and provide written informed consent Exclusion Criteria History of previous surgery on either knee Concomitant ligament injuries requiring surgical repair (e.g., PCL, MCL, LCL) Severe meniscal injury requiring repair or affecting rehabilitation progression Known cardiovascular, vascular, or thromboembolic disorders Peripheral vascular disease or conditions contraindicating blood flow restriction training Neurological disorders affecting lower limb function Uncontrolled systemic disease (e.g., uncontrolled diabetes or hypertension) Postoperative complications such as infection, deep vein thrombosis, or graft failure Inability to comply with the rehabilitation program or follow-up assessments
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Genom att skicka in godkänner du våra Användarvillkor
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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Cairo University
Cairo, Cairo Governorate, 11511, Egypt
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Physical Therapy
Giza, 12613, Egypt
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