Can a targeted nerve block cut opioid use after spine surgery?
NCT ID NCT04233736
First seen Sep 01, 2026 · Last updated Sep 02, 2026 · Updated 1 time
Summary
This trial tests whether a bilateral erector spinae plane block, an ultrasound-guided injection near the spine, can reduce pain and opioid use after lumbar or lumbo-sacral spine surgery. Half of the participants receive the block, while the other half receive a sham procedure. Researchers measure pain scores and opioid consumption during the hospital stay to see if the block helps.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Bilateral lumbar erector spinae plane block, an ultrasound-guided injection near the spine to numb nerves and ease pain
- What this could lead to
- If effective, this nerve block could offer a way to control pain after spine surgery with less reliance on opioids.
- What could go wrong
- This is an early-stage trial with a small number of participants, and the block may not reduce pain or opioid use as hoped. Risks include nerve damage, bleeding, or infection at the injection site.
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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.
- Started
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Jul 2021
- Expected to finish
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Jan 2022
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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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.
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: * Spine surgery at or below the L1 vertebral level * Midline surgical approach Exclusion Criteria: * Previous lumbar or lumbo-sacral surgery with or without hardware placement * Evidence of dura pathology (including CSF leak) * Spine tumor * Non-English speaking
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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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University of California San Francisco
San Francisco, California, 94143, United States
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