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New study aims to cut opioid use after spinal fusion

NCT ID NCT07228039

First seen Nov 15, 2025 · Last updated Jun 21, 2026 · Updated 28 times

Summary

This study tests whether a specific type of nerve block (ESP block) can reduce pain and the need for strong painkillers after spinal fusion surgery. 75 adults will be randomly assigned to receive either a standard painkiller (bupivacaine) or a longer-acting version mixed with liposomal bupivacaine. Researchers will measure pain scores, opioid use, and how quickly patients can get out of bed and go home.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Locations

  • Duke University

    Durham, North Carolina, 27710, United States

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

bupivacaine with or without liposomal bupivacaine

What this could lead to

If it works, this could point toward a better way to manage pain after spinal surgery, reducing the need for strong painkillers.

What could go wrong

This is a small, early-phase study (75 people) testing a well-known painkiller in a new way. It may not show a meaningful difference between the two approaches.

Conditions

The condition(s) this trial relates to.

Pain, Postoperative

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.