Can a targeted nerve block spare children from opioids after chest surgery?
NCT ID NCT07796399
First seen Sep 01, 2026 · Last updated Sep 02, 2026 · Updated 1 time
Summary
This trial tests two nerve block techniques to see which one better relieves shoulder pain in children after chest surgery. Researchers will compare pain scores, opioid use, and complication rates between the two blocks. The goal is to find a safer, more effective way to manage pain and reduce opioid side effects in young patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Two regional anesthesia techniques: an interscalene brachial plexus block and an anterior supraclavicular nerve block, both given during thoracic surgery to manage postoperative shoulder pain.
- What this could lead to
- If one block works better, it could become the standard for easing shoulder pain after chest surgery in children, reducing the need for opioids and their side effects.
- What could go wrong
- This is a mid-stage trial with 126 participants, so results may not apply to all children. Nerve blocks carry risks like infection, bleeding, or nerve damage, though these are uncommon.
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 2/3
Runs two stages together: whether the treatment works, then large-scale confirmation.
- Participants
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About 126 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2026
- Expected to finish
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Apr 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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5 to 18 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: * ASA physical status II-III * Elective open thoracotomy Exclusion Criteria: * Pre-existing shoulder pathology * Coagulopathy or infection at injection site * Allergy to local anesthetics * Neurological disorders involving upper limb
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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.
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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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Children's Cancer Hospital 57357
RECRUITINGCairo, Egypt, 11617, Egypt
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