Safer pain block could cut opioid use in lung surgery
NCT ID NCT06507293
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study compares two types of nerve blocks—paravertebral block and erector spinae plane block—to see which controls pain better during and after thoracotomy (lung surgery). The goal is to reduce the amount of opioids needed during surgery and improve recovery. Sixty adults scheduled for elective thoracotomy will be randomly assigned to receive one of the two blocks before surgery, and their pain levels and opioid use will be measured.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- bupivacaine
- What this could lead to
- If this works, it could show that a simpler, safer nerve block is just as effective for controlling pain during lung surgery, potentially reducing opioid use and speeding recovery.
- What could go wrong
- This is a small, early-stage study with only 60 participants, so results may not apply to everyone. The two blocks may turn out to be equally effective, or one may not work as well as hoped.
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.
- Started
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Aug 2024
- Expected to finish
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Dec 2025
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 to 65 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.
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: * Patients undergo elective thoracotomy surgery * ASA physical status I-III Exclusion Criteria: * Spinal deformities * BMI\>35 * Patiens \<50 kg * Allergies to study medications
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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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Kocaeli University
RECRUITINGKocaeli, 41350, Turkey (Türkiye)
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a nerve block stop pain months after hysterectomy?