Which nerve block eases Kids' pain after spleen surgery?
NCT ID NCT07336043
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests two types of nerve blocks to control pain in children aged 8 to 16 after laparoscopic spleen removal. Sixty children will receive either an external oblique intercostal block or a transversus abdominis plane block. Researchers will measure pain scores and heart rate to see which block 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
- nerve block procedure
- What this could lead to
- If one block works better, it could mean less pain and faster recovery for children after spleen surgery.
- What could go wrong
- This is a small, early study with only 60 children. Results may not apply to all patients or 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
-
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
-
About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Jan 2026
- Expected to finish
-
Jul 2026
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
-
8 to 16 years
- Sex
-
Anyone
- Healthy volunteers
-
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: * Children of both gender, * aged 8 to 16 years with American Society of Anesthesiologists Physical Status I to III, * who were scheduled for laparoscopic Splenectomy surgery. Exclusion Criteria: * Parents declined to participate in the trial. * Physical or developmental delay. * Pre-existing renal or cardiovascular disease, bone disease, or gastrointestinal disorders. * Infection at proposed injection sites. * Prior major abdominal surgery
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Tanta University
Tanta, Egypt
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