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Safer pain relief for kids? study tests two block techniques

NCT ID NCT07256535

Knowledge-focused Sponsor: Kocaeli University Source: ClinicalTrials.gov ↗

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This trial is taking on new participants right now.
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Registered, but not yet taking participants.
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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 Results may not be published yet.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.
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Cancelled before anyone took part.

Expanded access (not trials)

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First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at two pain-block methods—quadratus lumborum block (QLB) and transversus abdominis plane block (TAP)—in 20 children aged 1-6 having hernia surgery. The goal is to measure how much of the numbing drug bupivacaine gets into the blood after each method, since lower levels mean a lower risk of side effects. Researchers will also compare pain scores to see which block works better. The findings could help choose the safer and more effective technique for kids.

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 20 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jan 2026

An estimate. Start dates often move.

Expected to finish

Jun 2026

An estimate. End dates often move.

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

1 year to 6 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: * Patients undergoing elective inguinal hernia surgery. * 1-6 years of age * ASA I-II patients Exclusion Criteria: * Vulnerable populations such as those incapacitated, those in intensive care, those unconscious, those unable to give personal consent, or impressionable individuals will not be included in the study. * Although pediatric patients who may be considered a vulnerable population will be included in the study, patients with serious illnesses such as ASA III-IV will not be included in this group. * Patients who refuse to participate in the observational study, their parents/legal guardians, * Patients with incomplete data * Patients who underwent surgery with an incision other than the planned one for any reason.

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As listed by the trial registrant

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Blood bupivacaine concentration

How to take part

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Contacts and locations

Locations

  • Kocaeli University

    Kocaeli, Turkey (Türkiye)