Tiny yale study probes blood flow cuffs for ACL rehab
NCT ID NCT05012982
First seen Jun 25, 2026 · Last updated Aug 26, 2026 · Updated 3 times
Summary
This study tests whether using a special cuff to partly block blood flow during exercise can improve recovery after ACL reconstruction. Twenty adults will have two training sessions—one with the cuff inflated and one without—so researchers can compare changes in immune cells and energy use. The goal is to understand the body's response, not to prove a treatment works yet.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- AirBand (blood flow restriction device)
- What this could lead to
- If successful, this could help design better rehab programs for ACL patients by understanding how blood flow restriction affects recovery.
- What could go wrong
- This is a very small early study with only 20 participants, so results may not apply to everyone. It focuses on biological markers, not direct recovery outcomes.
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
-
18 people
The number who actually took part.
- Started
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Feb 2023
- Finished
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May 2026
- 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
-
18 to 60 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: 1. Provision of signed and dated informed consent form 2. Stated willingness to comply with all study procedures and availability for two study visits at least 1 week apart 3. All genders, between 18 and 60 years of age 4. In good general health without any underlying medical conditions or prior injury that would place the subject at risk of further injury/illness by participating in the study Exclusion Criteria: 1. Serious medical conditions including cardiovascular, metabolic (diabetes), rheumatologic, pulmonary, or musculoskeletal. 2. Multiple ligament ruptures or trauma 3. Rheumatoid arthritis or other significant comorbidities 4. Lower extremity vascular pathology, including history of deep vein thrombosis 5. Those with a history of sickle cell trait or disease 6. Use of anticoagulant medications 7. Pregnancy 8. Treatment with another investigational drug or other intervention within one month of Study Day 1 9. Current smoker or tobacco use within 3 months of Study Day 1 10. Febrile illness within 2 weeks of Study Day 1
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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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Gaylord Outpatient Physical Therapy North Haven Clinic
North Haven, Connecticut, 06473, United States
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Yale New Haven Hospital
Milford, Connecticut, 06461, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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