Tooth-Colored fillings face off: which works best for cavities?
NCT ID NCT06667271
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 Hide 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)
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