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Which nerve block eases Kids' surgery pain better? new study finds out

NCT ID NCT05671484

Symptom relief Sponsor: Namik Kemal University 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at two types of nerve blocks (TFP and QLB) to see which one works better for pain after lower belly surgery in children aged 3 to 7. The goal was to reduce pain and the need for extra pain medicine. 66 children took part, and researchers measured their pain scores and how much painkiller they needed.

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

66 people

The number who actually took part.

Started

Sep 2025

Finished

Feb 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

3 to 7 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: * Parental acceptation to participate and signed written consent * Aged between 3 and 7 * American Society of Anesthesiologists (ASA) physical score I or II * Elective infra umbilical surgery Exclusion Criteria: * Parental refusal to participate * Known allergy to local anesthetics * American Society of Anesthesiologists (ASA) physical score ≥ III * Coagulopathy * Hypersensitivity history to the agents to be used * Local infections * Known anatomically or systemic disorder * Known growth and developmental retardation

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Conditions

The condition(s) this trial relates to.

agnosia

As listed by the trial registrant

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

Surgical procedure, unspecified

Contacts and locations

Locations

  • Tekirdag Namik Kemal University

    Tekirdağ, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.