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Tooth repair showdown: which dental glue holds up best?

NCT ID NCT05361746

Disease control Sponsor: Solventum US LLC Source: ClinicalTrials.gov ↗

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 two dental adhesives (glues) used to repair small, non-cavity tooth damage near the gums. 38 adults each had two damaged teeth fixed, one with each adhesive, to compare how well they stayed in place and sealed the tooth. The goal was to see which glue works better for long-lasting repairs.

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

38 people

The number who actually took part.

Started

Aug 2022

Finished

Sep 2025

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

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: Subjects may be included that meet the following criteria: 1. Subject is at least 18 years of age at the time of consent 2. Subject is able to provide their own informed consent 3. Subject has a minimum of two teeth that: * have non-carious Class V lesions that are at least 1.5 mm deep * are not devitalized * have not undergone root canal treatment 4. Subject has an Approximal Plaque Index score ≤ 40% as assessed via explorer and without the use of plaque-disclosing agents 5. Subject is able and willing to return for all scheduled study visits 6. Subject meets the Level-I or Level-II classification criteria of the American Society of Anesthesiologists (ASA) Physical Status Classification System For Dental Patient Care Exclusion Criteria: Subjects may not be included that meet any of the following criteria: 1. Subject has any of the following: * rampant caries * chronic periodontitis * salivary gland dysfunction 2. Subject is unable, for any reason, to tolerate the procedure time required to place the restorations 3. Subject has unacceptable oral hygiene (eg, chronic moderate to heavy plaque accumulation along the gumline) 4. Subject has known sensitivity to the study product components (ie, acrylate) 5. Subject is planned to be enrolled in another investigational trial that requires additional interventions at any time during the study

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As listed by the trial registrant

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

Class V non-carious cervical dental lesions

Contacts and locations

Locations

  • Louisiana State University HSC-Health, School of Dentistry

    New Orleans, Louisiana, 70119, United States