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New dental shot may ease pain for kids with toothaches

NCT ID NCT07638254

Symptom relief Sponsor: Universidad Autonoma de San Luis Potosí Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tests whether a specially prepared (buffered) numbing shot works better than the standard shot to reduce pain and anxiety in children aged 6 to 12 who need a tooth filling or root canal for an infected baby tooth. Researchers will measure pain using a behavior scale, heart rate, and skin signals during the procedure. The goal is to make dental visits more comfortable 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 60 people

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

Started

Mar 2026

Expected to finish

Oct 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

6 to 12 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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 6 to 12 years * Diagnosis of irreversible pulpitis due to dental caries in primary maxillary molars * American Society of Anesthesiologists (ASA) Physical Status Classification I * Cooperative or definitely cooperative behavior according to Frankl Behavioral Scale (Frankl III or IV) * Written informed consent provided by parent or legal guardian, and child assent when applicable * No use of analgesic or anti-inflammatory medication within 24 hours prior to the procedure Exclusion Criteria: * Known allergy to any component of local anesthetic solution * History of negative or traumatic dental experiences within the previous 12 months that may interfere with behavioral assessment * Radiographic evidence of periapical pathology associated with the affected tooth * Presence of localized abscess or acute spreading infection at the injection site

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Conditions

The condition(s) this trial relates to.

pulpitis

As listed by the trial registrant

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

Pulpitis

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.

    Open the record ↗

  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

  • Universidad Autónoma de San Luis Potosí

    RECRUITING

    San Luis Potosí City, San Luis Potosí, 78290, Mexico

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