New beads could ease pain after spine surgery
NCT ID NCT07201987
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether placing special beads containing an antibiotic and pain relievers directly into the surgical site during spine surgery can improve recovery. About 100 adults having lumbar spine surgery will either get beads with just antibiotic or beads with antibiotic plus morphine and bupivacaine. Researchers will measure pain, medication use, and hospital stay length.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- vancomycin, morphine, and bupivacaine in calcium sulfate beads
- What this could lead to
- If it works, this could offer a new way to manage pain and prevent infection after spine surgery, potentially reducing the need for strong painkillers.
- What could go wrong
- This is a small, early-phase trial. The beads may not work better than standard care, and there is a risk of allergic reaction or infection.
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 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2027
An estimate. Start dates often move.
- Expected to finish
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Jan 2028
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.
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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: * Age ≥ 18 years * Able to understand and provide consent in English * Undergoing elective lumbar spinal decompression and fusion surgery at one or two levels Exclusion Criteria: * History of allergy or hypersensitivity to morphine, bupivacaine, or calcium sulfate. * Active systemic or localized infection at the surgical site. * History of chronic opioid dependence or opioid use disorder (as it may confound pain assessment). * Patients with severe renal or hepatic impairment (due to altered metabolism of analgesics and risk of complications from analgesic side effects). * Pregnant or breastfeeding individuals. * Filling of defects that are intrinsic to the stability of the bony structure * Severe vascular or neurological disease * Uncontrolled diabetes * Severe degenerative bone disease * Hypercalcemia
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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