New pain block cocktail may cut opioid use after breast surgery
NCT ID NCT07683416
First seen Jul 06, 2026 · Last updated Aug 25, 2026 · Updated 4 times
Summary
This trial compares two ultrasound-guided nerve blocks—serratus-intercostal and erector spinae—both using a mix of bupivacaine and dexmedetomidine to control pain after mastectomy. The goal is to see which block reduces the need for morphine and improves pain scores. Seventy women undergoing unilateral mastectomy will participate, with outcomes measured over the first 24 hours 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
- dexmedetomidine and bupivacaine
- What this could lead to
- If one block proves better, it could offer a more effective, opioid-sparing pain control method for mastectomy patients.
- What could go wrong
- This is a small, early-stage comparison; results may not apply broadly, and nerve blocks carry risks like infection or incomplete pain relief.
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
-
70 people
The number who actually took part.
- Started
-
Jun 2026
- Expected to finish
-
Feb 2027
An estimate. End dates often move.
- 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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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: * Unilateral mastectomy operations. * Body mass index less than 35 kg per square meter. * American Society of Anesthesiologists physical status grade I-II. Exclusion Criteria: * Patient refusal. * History of chronic pain therapy. * Infection at the injection site.
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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
-
Zagazig university hospital
Zagazig, Egypt
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Other studies related to the condition(s) this trial covers.
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