New pain block could cut opioid use in kidney stone surgery
NCT ID NCT07457983
First seen Jun 25, 2026 · Last updated Jul 21, 2026 · Updated 3 times
Summary
This study tests whether an erector spinae plane block, a type of nerve block, can reduce pain and the need for opioid painkillers after percutaneous nephrolithotomy, a surgery to remove large kidney stones. Sixty adults scheduled for this surgery will receive either the block plus standard anesthesia or standard anesthesia alone. Researchers will measure pain scores and total opioid use in the first 24 hours after surgery.
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 with bupivacaine
- What this could lead to
- If it works, this could offer a safer way to manage pain after kidney stone surgery, reducing the need for opioids.
- What could go wrong
- This is a small, early-stage trial with only 60 participants. The block may not provide significant pain relief, and results may not apply to all patients.
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
-
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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60 people
The number who actually took part.
- Started
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Apr 2026
- Finished
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Jun 2026
- 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. * American Society of Anesthesiologists (ASA) physical status I-II. * Scheduled for elective percutaneous nephrolithotomy under general anesthesia. * Able to understand the study procedures and provide written informed consent. Exclusion Criteria: * Age \< 18 years. * ASA physical status III-IV. * Refusal to participate in the study. * Known allergy or contraindication to local anesthetics (bupivacaine), opioids, or study medications. * Coagulopathy or anticoagulant therapy contraindicating regional block. * Infection at the injection site. * Severe psychiatric or cognitive disorder precluding reliable pain assessment or questionnaire completion.
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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
-
Adıyaman University Faculty of Medicine Anesthesiology and Reanimation
Adıyaman, Turkey (Türkiye)
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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