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Which pain block works best for Kids' surgery?

NCT ID NCT07256899

Symptom relief Sponsor: Istanbul University - Cerrahpasa Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study compared two types of pain blocks given before surgery to children aged 6 months to 12 years having lower belly or groin surgery. The blocks use numbing medicine to reduce pain after the operation. Researchers measured how much extra pain medicine the children needed and their pain scores. The goal is to find which block provides better pain relief and comfort for 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
bupivacaine
What this could lead to
If one block works better, it could lead to better pain control and less need for extra pain medicine in children after surgery.
What could go wrong
This is a small, completed study with only 68 children, so results may not apply to all kids or surgeries. Both blocks are already used, so no major breakthrough is expected.

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

68 people

The number who actually took part.

Started

Dec 2025

Finished

Mar 2026

Lead sponsor

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

6 months to 12 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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Age 6 months to 12 years * Scheduled for lower abdominal urogenital surgery (e.g., inguinal hernia repair, undescended testis surgery) * ASA physical status I-III * Parental/guardian informed consent obtained Exclusion Criteria: * Allergy to local anesthetics * Infection at the injection site * Coagulopathy or other contraindications to regional anesthesia * Laparoscopic orchiopexy scheduled * ASA physical status IV * Inability to obtain consent from parent/guardian * Expected need for postoperative intensive care

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Conditions

The condition(s) this trial relates to.

agnosia cryptorchidism

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Anesthesia and analgesia Pediatric anesthesia Pediatric regional anesthesia Regional anesthesia block

Contacts and locations

Locations

  • Istanbul University-Cerrahpasa, Cerrahpasa Medicine of Faculty

    Bakırköy, Istanbul, 34153, Turkey (Türkiye)

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