Nerve block showdown: which technique offers better pain control after knee surgery?
NCT ID NCT07700797
First seen Jul 14, 2026 · Last updated Jul 17, 2026 · Updated 2 times
Summary
This study compares two ultrasound-guided nerve block methods for controlling pain after knee surgery: an adductor canal block combined with infiltration of the back of the knee (IPACK) versus a 4-in-1 block. Researchers measure pain scores, how much extra pain medication is needed, and how long pain relief lasts. The goal is to find which technique provides better pain control and recovery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- nerve block (adductor canal block with IPACK or 4-in-1 block)
- What this could lead to
- If one technique proves better, it could lead to improved pain control and faster recovery after knee surgery.
- What could go wrong
- This is a small, early-stage study with only 24 participants, so results may not apply to all patients or surgeries.
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
-
24 people
The number who actually took part.
- Started
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Jun 2026
- Finished
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Jun 2026
- Lead sponsor
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A government agency
The lead sponsor is a government body.
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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21 to 64 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\. Patients or caregivers acceptance. 2. Age : 21 - 64 years 3. Sex : both ( males \& females). 4. Physical status: ASA І \& II. 5. BMI 18.5-30 kg/m2. 6. Type of operations : elective surgery. 7. Type of anesthesia: unilateral intrathecal anesthesia. 8. Patients undergoing elective knee surgery under unilateral spinal anesthesia 9. Duration of surgery within 2 hr. Exclusion Criteria: * Known history of allergy to study drug Coagulopathies or taking drugs affecting coagulation.. Contraindications for peripheral nerve block (PNB) and spinal anesthesia (SA) (coagulation defects, infection at the puncture site), bone degenerative disease and posttraumatic condition of the spine, dementia and severe visual or auditory disorder. Current severe psychiatric disease, alcoholism or drug dependence. Subjects with history previous knee surgery, osteoarthritis, malformation or tumors (including Baker's cyst), which could alter the normal anatomy of the popliteal fossa
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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
-
Faculty of Medicine, Zagazig University Hospitals
Zagazig, Sharqia Province, 055, Egypt
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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