A shot of numbing relief: could trigger point injections cut opioid use after neck surgery?
NCT ID NCT04640896
First seen Aug 13, 2026 · Last updated Aug 14, 2026 · Updated 1 time
Summary
This trial tests whether giving trigger point injections—small amounts of numbing medication into tender neck muscles—shortly after anterior cervical surgery can reduce pain and the need for opioid painkillers. Patients undergoing elective anterior neck surgery are randomly assigned to receive either the injections or standard pain management. The study measures pain levels and opioid use in the first 24 hours after the procedure.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Trigger point injections with bupivacaine, a numbing medication, given shortly after surgery
- What this could lead to
- If effective, this approach could offer a way to ease post-surgical neck pain and reduce reliance on opioid painkillers.
- What could go wrong
- This is a small, early-stage trial, and results may not apply to all patients. There is a risk of injection-related side effects, and the benefit over standard care is not yet proven.
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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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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60 people
The number who actually took part.
- Started
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Nov 2020
- Finished
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Oct 2023
- 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.
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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: * Elective anterior cervical surgery Exclusion Criteria: * Emergency surgery * Local anesthetic allergy * Long term opioid usage (not including tramadol and codeine) * Intra-operative complication (e.g. unstable cervical spine)
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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
-
George Washington University Hospital
Washington D.C., District of Columbia, 20037, United States
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