Which nerve block best cuts opioid use after mastectomy?
NCT ID NCT04016376
First seen Jun 27, 2026 · Last updated Sep 04, 2026 · Updated 1 time
Summary
This study tested three different nerve block methods to manage pain after a double mastectomy with immediate reconstruction. Over 1,500 women received either a paravertebral block, a serratus+PECS-1 block, or a combination. The goal was to see which approach reduces the need for opioid painkillers 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
- nerve blocks (local anesthesia)
- What this could lead to
- If successful, this could identify the best nerve block technique to reduce pain and opioid use after mastectomy, improving patient recovery.
- What could go wrong
- This is a completed Phase 4 study, so results are available. However, the best block may still leave some patients needing opioids, and individual pain responses vary.
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 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
1,507 people
The number who actually took part.
- Started
-
Jul 2019
- Finished
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Feb 2026
- 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
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
-
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: * Female patients \>/= 18 years old * Undergoing Bilateral Mastectomy with immediate reconstruction (BMw/IR) * Scheduled for surgery at Josie Robertson Surgical Center (JRSC) * Must be appropriate for an agree to receive a nerve block * Must be appropriate for randomization * Able to read and speak English * Willing and able to provide written informed consent Exclusion Criteria: * None applicable, as exclusion occurs prior to consent
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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
-
Memorial Sloan Kettering Cancer Center
New York, New York, 10065, United States
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