ACL surgery study halted: did tourniquet use matter?
NCT ID NCT05931627
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study aimed to see if using a tourniquet less during ACL reconstruction surgery helps patients recover quadriceps muscle function faster and with less pain. Only 1 person was enrolled before the trial was terminated, so no meaningful results were obtained. The study was designed to compare limited tourniquet use versus standard use in adults having ACL surgery with a patellar tendon graft.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could show that using a tourniquet less during ACL surgery helps patients recover quadriceps strength faster and with less pain.
- What could go wrong
- The trial was terminated early with only 1 participant, so no reliable conclusions can be drawn. Results may not apply to all ACL 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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1 person
The number who actually took part.
- Started
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Mar 2024
- Finished
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Feb 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
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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: 1. Patients undergoing an arthroscopic assisted ACLR using a bone-tendon-bone patellar tendon autograft. 2. 18 years or older 3. English speaking Exclusion Criteria: 1. Concomitant procedures (e.g., osteotomy or other ligamentous reconstructions) other than chondroplasty, partial meniscectomy or meniscal repair 2. Medical contraindications to epinephrine or TXA use. 3. Hemophilia or other predisposition for bleeding 4. Does not follow study protocol in regard to regional anesthesia, TXA, epinephrine use in the arthroscopy fluid and post-operative rehabilitation. 5. Participation in physical therapy at any facility other than the OrthoCarolina Randolph, Matthews or South Park locations
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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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OrthoCarolina Research Institute, Inc.
Charlotte, North Carolina, 28207, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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