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New study tests better fillings for Kids' cavities

NCT ID NCT06771362

Disease control Sponsor: Çanakkale Onsekiz Mart 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looked at two different bulk-fill materials used to repair cavities in children's baby molars using a gentle, drill-free method called atraumatic restorative treatment (ART). Researchers treated 127 children aged 4-9 and checked the fillings at 3, 6, and 12 months to see how well they held up in terms of function, appearance, and tooth health. The goal is to find out which material works best for kids' teeth.

What this could mean

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

Active substance
Bulk-fill composite and high-viscosity glass ionomer cement
What this could lead to
If successful, this could help dentists choose better materials for filling cavities in children's baby teeth, leading to longer-lasting and more comfortable restorations.
What could go wrong
This is a small, completed study with only 127 children, and results may not apply to all kids or tooth types. The follow-up is only 12 months, so long-term success is unknown.

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

127 people

The number who actually took part.

Started

Jan 2025

Finished

Jan 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

4 to 9 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: 1. Patients and parents of the patients who accept to participate and sign the informed consent. 2. Children between the ages of 4-9 3. Healthy children without a history of serious systemic conditions necessitating chronic use of medications. 4. Children whose dental examination reveals at least one untreated asymptomatic cavitated carious lesion (ICDAS II index: code 4,5,6) affecting primary molars. 5. Absence of former history of spontaneous pain from the offending tooth/teeth. 6. Patients with an appropriate level of cooperation to complete treatment under clinical conditions. 7. Teeth are in a restorable condition. Natural exfoliation of primary teeth to be treated should not be expected within two years. Exclusion Criteria: 1. Patients and parents of the patients who does not accept to participate and sign the informed consent 2. Patients with special health care needs or any medical conditions. 3. Primary molar teeth with excessive crown damage that cannot be restored. 4. Primary molar teeth in which bone loss exceeds 1/3 of the roots. 5. Primary molar teeth that have previously undergone root canal treatment or pulpotomy treatment. 6. Presence of internal/external and root resorption in primary teeth to be treated. 7. Root fracture, ankylosis or mobility in the primary teeth to be treated.

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Conditions

The condition(s) this trial relates to.

dental caries dentin caries Stomatognathic Diseases Tooth Demineralization

As listed by the trial registrant

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

Dentin caries

Contacts and locations

Locations

  • Canakkale Onsekiz Mart University

    Çanakkale, Kepez, 17100, Turkey (Türkiye)

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