New nerve block technique could make mastectomy pain control safer
NCT ID NCT02911168
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study compares two types of ultrasound-guided nerve blocks for controlling pain after mastectomy: the standard paravertebral block and a newer proximal intercostal block. Researchers want to see if the newer block offers better needle visibility, faster procedure time, and improved safety. The study involves 20 women scheduled for mastectomy.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ultrasound-guided nerve block (proximal intercostal block or paravertebral block)
- What this could lead to
- If successful, this could show that the proximal intercostal block is a safer, easier-to-perform option for controlling pain after mastectomy.
- What could go wrong
- This is a very small, early-stage study with only 20 participants, so results may not apply to all patients or settings. The study focuses on imaging quality and procedure time, not long-term 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
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20 people
The number who actually took part.
- Started
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Sep 2016
- Finished
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Jan 2020
- 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 to 85 years
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: 1. Females age 18-85 years old 2. ASA 1-3 3. Patient scheduled for unilateral or bilateral mastectomy with or without reconstruction Exclusion Criteria: 1. Coagulopathy 2. Patient refusal 3. Allergy to local anesthetics
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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
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Brigham and Women's Hospital
Boston, Massachusetts, 02115, United States
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