Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

NYU dentists put new tooth-colored filling to the test for smile makeovers

NCT ID NCT07128589

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tests how well a new flowable composite material (3M Filtek Supreme) works for fixing front teeth (class IV cavities) and making veneers. About 75 adults will get the material and be checked at 7 days, 6, 12, and 24 months to see if the repair lasts and looks good. The goal is to see if this material is a reliable option for dental restorations.

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 75 people

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

Started

Aug 2025

Expected to finish

Sep 2028

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 to 75 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: * Age between 18 -75 years old * must be willing and able to provide informed consent to participate in the study * must be available for the required post-operative follow-up study visits * must be in good general health * must be in good oral health hygiene (FMPS \< 20%) * have at least 6 anterior maxillary teeth * Central and lateral incisors with class IV or Veneer indications. Veneers will be performed exclusively with its contralateral teeth (pairs). Exclusion Criteria: * Single tooth veneers * Canines * Periodontal disease * Pulpal diseases * Occlusal dysfunctions (end-to-end bite) * Lack of occlusal stability * Missing posterior teeth, affecting the occlusal distribution * Study tooth, adjacent tooth, or opposing tooth with mobility \> grade 2 using the Miller's tooth mobility index * Systemic or local disorders that contra-indicate the dental procedures needed in this study * Rampant, uncontrolled caries * Heavy use of smoking tobacco (1 pack or equivalent a day) or chewing tobacco * Evidence of xerostomia * Evidence of severe bruxing or clenching, or in need of Temporomandibular Joint (TMJ) related therapy * Known allergic reaction and/or sensitivity to research materials being used * Condition or history of chronic use of anti-inflammatory, analgesic (pain), and/or mind altering drugs for medical (including psychiatric) and pharmacotherapeutic therapies that might alter the perception of pain * Tooth surface loss (attrition, erosion, abrasion, or abfraction) on study tooth or adjacent teeth that could impact the perception of pain. * Taking part in a clinical evaluation of any other dental material * In the opinion of the Investigator, unsuitable for enrollment in the study for reasons other than those specified in the above exclusion criteria * Pregnant at the time of enrollment or procedure visit (determined by urine pregnancy test).

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Dental restoration are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

As listed by the trial registrant

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

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • NYU College Of Dentistry

    RECRUITING

    New York, New York, 10010, United States

More trials for these conditions

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