Could magnesium make mastectomy recovery less painful?
NCT ID NCT07434232
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether adding magnesium sulfate to a standard nerve block can better control pain after a mastectomy. One hundred women having breast cancer surgery will be randomly assigned to receive the nerve block with or without magnesium. The main goal is to see if it reduces the need for opioid painkillers in the first 24 hours after surgery.
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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 100 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Feb 2026
An estimate. Start dates often move.
- Expected to finish
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Apr 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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30 to 75 years
- Sex
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Female participants only
- 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.
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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: * Female patients aged 30 to 75 years diagnosed with non-metastatic breast cancer and scheduled for modified radical mastectomy. * ASA, I-III and NYHA, I-II. * Written informed consent. Exclusion Criteria: * ASA physical status \>III and NYHA \>II, * body mass index \>40 kg/m2, * pregnant women, * Patients with organ failure or coagulation disorders. * Allergy to local anesthetics or magnesium sulfate * Contraindications as local infection * History of chronic pain or opioid use . * Unwilling to participate in the study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
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The official record
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A doctor treating you
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