New tooth fillings put to the test in 5-year study
NCT ID NCT06369779
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests two new dental filling materials for cavities in back teeth. 65 adults with cavities or old fillings that need replacing will receive the new fillings and be checked for pain, function, and appearance over 5 years. The goal is to see if the materials are safe and work well.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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
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65 people
The number who actually took part.
- Started
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May 2024
- Expected to finish
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Dec 2030
An estimate. End dates often move.
- Lead sponsor
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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
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Informed Consent signed by the subject * Age: 18-65 years * Indication Class I or II direct restorations in premolars or molars (Replacement of insufficient fillings due to secondary caries, fractures, insufficient marginal adaptation, loss of filling or primary caries) * Cavity width must be at least half of the cusp tip distance * Vital teeth, regular sensitivity * Sufficient language skills * No active periodontits * Preoperative VAS (visual analogue scale) values \< 3 regarding tooth sensitivity and biting Exclusion Criteria: * Sufficient isolation of the cavity not possible * Not completed hygiene phase or poor oral hygiene * Missing antagonist, non-occlusion * Missing tooth adjacent to the tooth to be treated * Restorations replacing more than 1 cusp * Caries profunda or very deep cavity * Patients with a proven allergy to ingredients of the used materials (methacrylates) or local anesthetics (Articain, sulfite) * Patients with severe systemic diseases * Pregnancy
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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
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Ivoclar Vivadent AG
Schaan, Liechtenstein, 9494, Liechtenstein