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New dental fillings put to the test in small study

NCT ID NCT07394751

Knowledge-focused Sponsor: Ege 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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 compares four different dental filling materials in 20 patients with cavities in their back teeth. The fillings are evaluated over 9 months for how well they hold up, look, and affect tooth health. The goal is to see if newer bioactive materials perform better than standard ones.

What this could mean

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

Active substance
dental filling materials (Tetric N-Ceram Bulk-fill, Stela, Cention Forte, Activa BioActive Restorative)
What this could lead to
If successful, this could help dentists choose better filling materials that last longer and cause fewer problems.
What could go wrong
This is a small, early-stage study with only 20 patients and a short follow-up of 9 months. Results may not apply to everyone or predict long-term performance.

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

20 people

The number who actually took part.

Started

Nov 2024

Expected to finish

Nov 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

20 to 34 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: * Individuals over the age of 16 with permanent dentition * Individuals with a total of four vital molar teeth requiring restoration (ICDAS 3-4), two on each side of the same jaw * Individuals with posterior contact with antagonist teeth * Individuals who are reliable, cooperative, and willing to participate in periodic follow-ups Exclusion Criteria: * Individuals whose antagonist teeth were missing or have crowns, bridges, etc. * Individuals with history of alcohol, drug, or medication addiction. * Individuals with pulp exposure during cavity preparation or a cavity depth exceeding 2-4 mm. * Individuals known to be unable to attend follow-up appointments. * Individuals with allergies to the products used in the procedure. * Individuals with severe tooth grinding or bruxism. * Individuals with caries conditions classified as ICDAS 5 and 6. * Pregnant or breastfeeding individuals and individuals planning pregnancy during the study.

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Conditions

The condition(s) this trial relates to.

dental caries

As listed by the trial registrant

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

Dental adhesive materials Dental caries

Contacts and locations

Locations

  • Ege University School of Dentistry

    Izmir, Bornova, 35100, Turkey (Türkiye)

More trials for these conditions

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