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Tooth-Colored fillings face off: which works best for cavities?

NCT ID NCT06667271

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested two types of tooth-colored fillings for cavities in back teeth: direct composite (placed directly in the tooth) and indirect composite (made in a lab and then cemented in). 90 adults with cavities received one of the two fillings. Researchers checked how well the fillings held up using standard dental criteria. The goal was to see which option works better for larger cavities.

What this could mean

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

Active substance
composite resin (direct and indirect)
What this could lead to
If successful, this could help dentists choose the best filling material for large cavities, balancing durability and cost.
What could go wrong
This is a small, completed study with only 90 participants. Results may not apply to everyone, and long-term outcomes beyond the study period are 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.

Participants

90 people

The number who actually took part.

Started

Mar 2023

Finished

Nov 2025

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 characteristics of the teeth were recorded prior to any restorative procedures. Periapical radiographs were used to assess the status and extent of caries, as well as to identify any potential periodontal or periapical pathologies that might necessitate endodontic treatment. The treated teeth were vital, asymptomatic, and in occlusal contact. Indirect composite restorations were applied to teeth that had caries, old composite or amalgam restorations, secondary caries, or teeth with cuspid loss where the isthmus width exceeded two-thirds of the intercuspal distance.

Ages

18 years and older

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: * They have been informed about the study and have agreed to participate. * They are over 18 years old. * They do not have any systemic diseases. * They maintain good general oral health. * They are not pregnant or breastfeeding. * The relevant tooth is vital, and the decay is at least 0.5 mm away from the pulp, as confirmed by radiographic findings. * There is a tooth in contact with the relevant tooth and an antagonist tooth. * They have agreed to attend follow-up appointments. Exclusion Criteria: * After being informed about the study, the participant declined to participate. * The individual is under 18 years of age. * The volunteer has a severe systemic disease. * They have active periodontal or pulp disease. * They have received endodontic treatment. * They experience bruxism.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • 53020

    Rize, Central, 53020, Turkey (Türkiye)

More trials for these conditions

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