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3-Second fillings: new dental material tested for speed and comfort

NCT ID NCT04686422

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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

Summary

This study tested a new dental filling material that hardens in just 3 seconds using a special light. 39 people with cavities or old fillings that needed replacement received the new filling. Researchers checked for pain, sensitivity, and how well the fillings held up over time.

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

39 people

The number who actually took part.

Started

Dec 2017

Finished

Jun 2021

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

19 to 90 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: * Each subject must need at least 1 restoration in a vital posterior tooth * Must have given written consent to participate in the trial * Replacement of defective restorations (i.e. fractured, stained, unaesthetic) with or with-out caries are acceptable * Must be available for the required follow-up visits over 3 years * Restored teeth must have occlusal contact with opposing teeth or restored teeth * Restoration width should be equal to or greater than 1/3 the distance from buccal to lin-gual cusp tips * 75% of the restorations Class II (minimum) and 25% Class I * Each Class II will have at least one proximal contact * 75% in molars (minimum) and 25% in premolars * All restored teeth must have at least one occlusal contact in habitual closure * Must have 20 or more teeth Exclusion Criteria: * If they have an allergy to ingredients of the materials under investigation (monomers) * Do not meet all inclusion criteria above * Have severe medical complications (organ transplants, long term antibiotic or steroid treatment, cancer or are immunocompromised) or disabilities meaning they may not be able to tolerate the time required to complete the restorations or to provide adequate oral hygiene * Have xerostomia either by taking medications known to produce xerostomia or those with radiation-induced xerostomia or Sjogren's syndrome - as dry mouth increases tooth and restoration wear as well as the development of caries. * Have teeth with advanced or severe periodontitis, rampant caries or poor oral hygiene which may require extraction of the teeth to be restored * Present with any systemic or local disorders that contraindicate the dental procedures included in this study * Have unstable occlusion * Have severe grinding/bruxing or clenching or need TMJ-related therapy * Have tooth with exposed pulp during preparation or caries removal * Teeth that are non-vital or that exhibit signs of pulpal pathology for restoration * Teeth that require cuspal build-ups involving more than one cusp

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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

  • UAB School of Dentistry

    Birmingham, Alabama, 35294-0007, United States

More trials for these conditions

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