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Dental adhesive showdown: which bond works best for tooth repair?

NCT ID NCT07459374

Disease control Sponsor: Hacettepe University 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 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study compares three different dental adhesives used to fill non-carious cervical lesions, which are tooth defects not caused by cavities. Thirty healthy adults aged 18-55 will receive restorations using one of the adhesives, and the team will check how well they hold up after 12 months. The goal is to find which adhesive performs best in terms of survival and quality.

What this could mean

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

Active substance
dental adhesive (G2 Bond Universal, Scotchbond Universal Plus, Tokuyama Universal Bond II)
What this could lead to
If successful, this trial could identify which dental adhesive is most effective for repairing tooth lesions, improving dental restoration outcomes.
What could go wrong
This is a small, early-stage trial with only 30 participants, so results may not apply to everyone. The study only lasts 12 months, so long-term performance is 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.

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

30 people

The number who actually took part.

Started

Mar 2024

Expected to finish

Mar 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 55 years

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: * Healthy individuals aged 18-55 years * No systemic condition contraindicating restorative treatment * Brushing teeth at least twice daily * At least 20 teeth in occlusion * At least three vital posterior teeth with non-carious cervical lesions and antagonist teeth * Completed initial periodontal therapy * Signed informed consent Exclusion Criteria: * Healthy individuals aged 18-55 years * No systemic condition contraindicating restorative treatment * Brushing teeth at least twice daily * At least 20 teeth in occlusion * At least three vital posterior teeth with non-carious cervical lesions and antagonist teeth * Completed initial periodontal therapy * Signed informed consent

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Conditions

The condition(s) this trial relates to.

tooth disorder

As listed by the trial registrant

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

Cervical lesion DENTAL

Contacts and locations

Locations

  • Hacettepe University

    Ankara, 06100, Turkey (Türkiye)

More trials for these conditions

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