A common mineral may boost pain relief after breast cancer surgery
NCT ID NCT07789600
First seen Aug 27, 2026 · Last updated Sep 01, 2026 · Updated 3 times
Summary
This trial tests whether adding magnesium sulfate to a standard local anesthetic, bupivacaine, can improve pain control after a mastectomy with lymph node removal. About 70 adult women undergoing this surgery will receive either the magnesium combination or the standard anesthetic alone, injected into the wound during the operation. Researchers will measure pain levels and painkiller use over the first 24 hours, with a follow-up safety check one to two weeks later. The goal is to see if this simple addition can reduce postoperative pain and the need for stronger pain medications.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Magnesium sulfate added to bupivacaine for local wound infiltration
- What this could lead to
- If it works, this could offer a simple, safe way to ease pain after mastectomy and reduce the need for opioid painkillers.
- What could go wrong
- This is a small, early-stage trial, and the benefit may be modest. Magnesium can cause side effects like low blood pressure or nausea, and results may not apply to all 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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About 70 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2028
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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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: * Adult female patients (age ≥18 years) undergoing elective modified radical mastectomy (MRM) with axillary clearance. * ASA physical status I-III. * Willingness to participate and provide informed consent. Exclusion Criteria: * Allergy to bupivacaine or magnesium. * Chronic opioid use or pre-existing chronic pain conditions. * Significant renal or hepatic impairment. * Pregnancy or lactation. * Neuromuscular disorders. * Abnormal baseline serum magnesium levels (e.g., hypermagnesemia).
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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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King Hussien Cancer Centre
Amman, Jordan
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Other studies related to the condition(s) this trial covers.
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- Magnesium boosts pain relief after breast surgery, study finds