Magnesium boost for knee surgery pain relief?
NCT ID NCT06520475
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether adding magnesium to the anesthetic bupivacaine for a nerve block around the knee provides better pain relief after total knee replacement surgery. 94 adults undergoing knee replacement were randomly assigned to receive either bupivacaine with magnesium or bupivacaine alone. The goal was to see if the combination reduces pain scores, delays the first request for additional pain medication, and lowers opioid use.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- bupivacaine and magnesium sulfate
- What this could lead to
- If adding magnesium works better than bupivacaine alone, it could offer longer-lasting pain relief after knee replacement surgery and reduce the need for strong painkillers.
- What could go wrong
- This is a small, completed study with only 94 participants. The results may not apply to all patients, and magnesium could cause side effects like low blood pressure or muscle weakness.
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
-
Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
-
94 people
The number who actually took part.
- Started
-
Aug 2024
- Finished
-
Oct 2025
- Lead sponsor
-
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 70 years
- Sex
-
Anyone
- Healthy volunteers
-
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: * American Society of Anesthesiologist (ASA) I or II physical status. * Between 18 and 70 years of age. * Both genders. * Patients undergoing total knee replacement surgery. Exclusion Criteria: * Patient refusal. * ASA Ⅲ and Ⅳ patients. * Known allergy to the study drugs. * Hypermagnesemia. * Central or peripheral neurological disease. * Pregnancy. * Drug or alcohol abuse. * Localized infection at the site of the block. * Bleeding disorder (platelets count less than 100,000 or international normalized ratio more than 1.4)
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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
-
Kasr Alaini hospital
Cairo, Egypt
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Other studies related to the condition(s) this trial covers.
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