Back surgery pain relief: does a Two-Level nerve block beat a Single-Level one?
NCT ID NCT07363096
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compares two ways of giving a nerve block (erector spinae plane block) to control pain after lumbar fusion surgery. Sixty adults undergoing back surgery will be randomly assigned to receive either a single-level or a two-level injection. Researchers will measure pain scores, opioid use, and side effects in the first 24 hours after surgery to see which method works better.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Erector spinae plane block (nerve block injection)
- What this could lead to
- If it works, this could show that a two-level nerve block provides better pain relief after lumbar fusion surgery than a single-level block.
- What could go wrong
- This is a small, early-stage trial with only 60 patients. It may not find a clear difference between the two techniques, and results may not apply to all spine surgeries.
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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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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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Feb 2026
An estimate. Start dates often move.
- Expected to finish
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Jan 2027
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
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 80 years
- 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: * ASA I-II-III, * BMI:18-40, * Patients undergoing lumbar stabilization surgery involving 2 to 4 vertebral levels * Patients who personally provide written informed consent to participate in the study Exclusion Criteria: * Patients with chronic pain conditions * Patients with a history of chronic opioid use * Patients undergoing emergency lumbar stabilization surgery
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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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.
Contacts and locations
Locations
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Ankara Etlik City Hospital
Ankara, Yenimahalle, 06170, Turkey (Türkiye)
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Chest surgery pain study seeks best relief strategy
- New study tests two injections to ease knee surgery pain and cut opioid use
- Eye-Opening pain relief: pupillometer may cut opioid use after surgery
- Hip surgery pain relief: which nerve block method works best?
- New pain block after back surgery shows promise