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Could a simple numbing shot before dental surgery prevent Kids' Post-Anesthesia confusion?

NCT ID NCT07604337

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 This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 will test whether giving children a local anesthetic (numbing medicine) in their gums before dental work under general anesthesia helps them wake up more calmly and with less pain. Eighty children aged 7 to 12 will be randomly assigned to receive the numbing shot or not. Researchers will measure confusion, pain, and recovery quality in the first 30 minutes after surgery.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
articaine hydrochloride with epinephrine
What this could lead to
If it works, this could provide a simple way to help children wake up more calmly and comfortably after dental surgery.
What could go wrong
This is a small, early-stage trial with only 80 children, so results may not apply to everyone. The benefit may be small or not noticeable.

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 80 people

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

Expected to start

Jun 2026

An estimate. Start dates often move.

Expected to finish

Dec 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

7 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: * Children aged 7 to 12 years * ASA physical status I or II * Scheduled for ambulatory dental treatment under general anesthesia * Ability to understand and respond to age-appropriate pain and recovery assessment tools * Written informed consent obtained from a parent or legal guardian * Child assent obtained when appropriate Exclusion Criteria: * Known allergy or contraindication to local anesthetic agents * Developmental delay or cognitive impairment preventing assessment * Autism spectrum disorder or severe behavioral disorder * Neurological disease affecting behavior or consciousness * Chronic analgesic or sedative medication use * Severe hepatic, renal, cardiac, or respiratory disease * Emergency dental procedure * Need for postoperative hospital admission * Inability to complete postoperative assessment tools

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Conditions

The condition(s) this trial relates to.

delirium Emergence Delirium

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.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. 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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  3. 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

  • Erciyes University Faculty of Dentistry

    Kayseri, Kayseri, 38039, Turkey (Türkiye)

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