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Lavender and high-tech needles: a new way to calm kids at the dentist?

NCT ID NCT07547371

Symptom relief Sponsor: Arzu Pınar Erdem 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 aromatherapy (lavender and orange oils) and digital anesthesia can reduce pain and anxiety in children aged 6-12 during tooth extractions. Researchers will compare these methods to traditional anesthesia to see which is more comfortable and less stressful. The goal is to find gentler, child-friendly approaches for dental procedures.

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 132 people

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

Started

Dec 2025

Expected to finish

Jul 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: Participants will be recruited from the Department of Pediatric Dentistry at Istanbul University Faculty of Dentistry who meet the following criteria: Children aged 6-12 years, Indicated for extraction of a mandibular primary molar without acute infection or abscess, No use of analgesic or sedative medications within the previous 24 hours, Absence of any systemic disease, Behavior rated as Category 2, 3, or 4 on the Frankl Behavior Rating Scale, Voluntary agreement to participate in the study. Exclusion Criteria: Children with a history of systemic disease or those taking medications on a regular basis, Known allergy to local anesthetic agents or essential oils, Use of analgesic or sedative medications within the previous 24 hours, Children with asthma, chronic obstructive pulmonary disease (COPD), upper respiratory tract infections, or any respiratory condition that may increase sensitivity to inhalational therapies, Children rated as Category 1 on the Frankl Behavior Rating Scale, indicating an inability to cooperate, Teeth indicated for extraction due to acute infection or abscess, Patients with teeth presenting mobility, ankylosis, or root resorption exceeding one-third of the root length.

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Conditions

The condition(s) this trial relates to.

Pain Toothache

As listed by the trial registrant

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

Dental anxiety Pain Tooth extraction

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

  • Istanbul University, Faculty of Dentistry, Department of Pediatric Dentistry

    RECRUITING

    Istanbul, Istanbul, 34093, Turkey (Türkiye)

More trials for these conditions

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