Nerve block before ACL surgery could help teens recover faster
NCT ID NCT06875427
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether a numbing injection (nerve block) given before ACL knee surgery helps teens recover better. About 38 participants aged 10-18 will either get the block plus standard anesthesia or standard anesthesia alone. Researchers will measure recovery quality, pain, opioid use, and satisfaction up to 6 weeks after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ropivacaine and dexmedetomidine
- What this could lead to
- If it works, this could show that a simple nerve block before ACL surgery helps teens recover faster with less pain and fewer opioids.
- What could go wrong
- This is a small feasibility trial with only 38 participants, so results may not apply to everyone. The block may not improve recovery and carries rare risks like nerve injury or allergic reaction.
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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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 38 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2025
- Expected to finish
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Jan 2027
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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10 to 18 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.
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: * Patients ASA I, II and III * 10-18 years of age * scheduled for ACL reconstruction * agreeable to regional block and follow-ups Exclusion Criteria: * Contraindications to adductor canal block. * Patients with coagulopathies, preexisting neurologic deficit * Significant comorbidities that may impact recovery or interfere with the study. * Refusal to regional techniques. * Moderate to severe cognitive deficit (patients who are unable to complete the questionnaire) * Patients with history of malignant hyperthermia
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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.
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
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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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McMaster Children's Hospital, Hamilton Health Sciences
RECRUITINGHamilton, Ontario, L8N 3Z5, Canada
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Nerve block showdown: which technique offers better pain control after knee surgery?
- Robotic knee tester aims to outdo the human hand in measuring ACL injuries
- Can a simple test predict ACL tears in teen soccer stars?
- AI learns to spot clean surgical zones in ACL repair
- Silence in the OR: headphones may speed up knee surgery
- Teens' ACL pain: which nerve block works best?