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Can a better numbing gel make dental shots less scary for kids?

NCT ID NCT07733622

What the study statuses mean

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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 Results may not be published yet.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
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Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jul 29, 2026 · Last updated Jul 30, 2026 · Updated 1 time

Summary

Dental injections are a major source of fear for children, but numbing gels and sprays may help. This study compares four common topical anesthetics—benzocaine spray, benzocaine gel, lidocaine spray, and lidocaine gel—to see which one best reduces pain and anxiety in 160 children aged 6 to 8 years. Researchers will measure children's self-reported pain, anxiety levels, and physical responses during routine dental treatment.

What this could mean

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

Active substance
topical anesthetic agents (benzocaine spray, benzocaine gel, lidocaine spray, lidocaine gel)
What this could lead to
If one formulation proves superior, it could help dentists choose the best option to ease children's fear and pain during routine dental procedures.
What could go wrong
This is an observational study, not a randomized trial, so results may be influenced by clinician choice. The findings may not apply to all children or dental situations.

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.

Participants

About 160 people

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

Expected to start

Jul 2026

An estimate. Start dates often move.

Expected to finish

Sep 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.

Who is studied

The study population will consist of healthy children aged 6-8 years who attend the Department of Pediatric Dentistry at Recep Tayyip Erdoğan University Faculty of Dentistry for routine dental treatment and require maxillary infiltration anesthesia for treatment of a maxillary second primary molar. Only children meeting the eligibility criteria and whose parents or legal guardians provide written informed consent will be enrolled.

Ages

6 to 8 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 8 years. * Frankl Behavior Rating Scale score of 3 or 4. * No previous history of local anesthetic injection for dental treatment. * Requiring maxillary infiltration anesthesia for treatment of a maxillary second primary molar. * Requiring non-emergency, painless dental treatment. * Medically healthy children with no chronic systemic disease, mental disability, or physical disability. * Written informed consent obtained from a parent or legal guardian. Exclusion Criteria: * Frankl Behavior Rating Scale score of 1 or 2. * Physical or intellectual disability. * History of cardiovascular disease, diabetes mellitus, Graves' disease, epilepsy, hyperthyroidism, active infection, phenylketonuria, cardiovascular shock, otorrhea, or otitis. * Known hypersensitivity or allergy to benzocaine, lidocaine, or any component of the topical anesthetic formulations. * Emergency dental treatment or presence of dental pain requiring urgent intervention. * Chronic liver or kidney disease. * History of methemoglobinemia.

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As listed by the trial registrant

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