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One-Shade wonders? study tests if universal composites can replace traditional fillings

NCT ID NCT06563128

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 26, 2026

Summary

This study compares four new single-shade universal resin composites to a conventional composite for filling class 2 cavities (between teeth). 45 adults will receive 180 fillings, which will be evaluated at 6 and 12 months by blinded dentists using standard criteria. The goal is to see if these simpler, color-matching materials perform as well as traditional options.

What this could mean

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

Active substance
dental composite resin
What this could lead to
If successful, this study could show that single-shade universal composites work as well as traditional ones, simplifying tooth filling procedures.
What could go wrong
This is a small, short-term study (45 people, 12 months) comparing materials, not testing a new treatment. Results may not apply to all cavity types or longer timeframes.

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 45 people

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

Started

Aug 2024

Expected to finish

Nov 2025

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

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: * The patient should not have any systemic disease. * You must be 18 years of age or older. * The patient must have good periodontal health. * Must have acceptable oral hygiene. * The teeth to be restored must be symptom-free and vital. * The mesial and distal surfaces of the teeth to be restored must be in contact with the proximal teeth. * The tooth to be restored must be in occlusion with its antagonist. * The tooth to be restored must have a class 2 caries lesion radiographically not exceeding 2/3 of the dentin. * Patients with caries have an ICDAS 3-4 score. * Voluntary acceptance to participate in the study after being informed about the study. Exclusion Criteria: * The patient has any systemic disease. * Previously adhered restoration and endodontic treatment on the tooth to be restored. * Poor periodontal health of the patient. * Poor oral hygiene. * The patient is pregnant or breastfeeding. * The patient is undergoing orthodontic treatment. * The patient has bruxism (tooth clenching) and a dry mouth. * The teeth are devitalised. * The patient refused to participate in the study after being informed about the study.

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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

  • Ataturk University Faculty of Dentistry Department of Restorative Dentistry Clinic

    Erzurum, 25050, Turkey (Türkiye)

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