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Recruiting NCT06960070

Clinical Success of Onlays Fabricated With Different Types of Resin

No phase Interventional Endodontically-Treated Teeth

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Saremco print resin, Varseosmile Crownplus resin, Varseosmile TriniQ resin.
Who it may be relevant to
Registry conditions: Endodontically-Treated Teeth. Basic parameters: 18 years — 84 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

One-year Clinical Evaluation of Onlay Restorations Fabricated With Three Different Additive Manufacturing Resins in Endodontically Treated Teeth: A Prospective Study

Overview

Additive manufacturing, also referred to as "3D printing" or "rapid prototyping," is defined as the process of joining materials layer by layer to create an object based on 3D model data. In this method, a digital data set is first created on a computer (computer-aided design, CAD) and then transferred to a 3D printer. The designed object is produced by printing it in successive layers. In contrast, in subtractive manufacturing, restorations are produced by milling homogeneous blocks based on computer-designed models. Compared to subtractive manufacturing technology, additive manufacturing allows for the production of more complex, detailed, and larger structures with much less material waste and without excessive use of force. It is thought that additive manufacturing has the potential to overcome the disadvantages of subtractive manufacturing. Over the past decade, global sales of industrial and personal 3D printers, materials, and services have increased by more than 33% annually. Due to its success in the production of surgical guides, temporary and permanent restorations, crowns and bridges, occlusal splints, frameworks, and orthodontic appliances, this technology has attracted significant interest in the field of dentistry. Although additive manufacturing has started to be used as an alternative to subtractive manufacturing in many applications, there is still a lack of information regarding the chemical composition, mechanical, and physical properties of printable resins. Moreover, clinical data on the use of these resins in permanent restorations are quite limited. Therefore, the aim of this study is to clinically evaluate and monitor for one year the performance of onlay restorations fabricated with three different resins of varying compositions in endodontically treated teeth.

Interventions

  • Device Saremco print resin
    The teeth were restored with Saremco print resin via Asiga Max printer according to the manufacturer's instructions.
  • Device Varseosmile Crownplus resin
    The teeth were restored with Varseosmile Crownplus resin via Asiga Max printer according to the manufacturer's instructions.
  • Device Varseosmile TriniQ resin
    The teeth were restored with Varseosmile TriniQ resin via Asiga MAx printer according to the manufacturer' instructions

Primary outcome measures

  • Clinical performance [Time frame: Baseline- 6 months-12 months]

Eligibility criteria

Inclusion criteria

  • Molar teeth that have undergone root canal treatment
  • Teeth with proximal defects located above the gingival margin
  • Defects limited to the occlusal surface and a single adjacent surface
  • Presence of an occlusal defect extending over one-third of the distance between the fissure and the cusp tip and involving one or more cusps
  • Presence of an opposing tooth or a fixed prosthetic restoration against the tooth to be restored
  • Presence of adjacent teeth next to the tooth to be restored

Exclusion criteria

  • Fractured or cracked teeth
  • Patients with temporomandibular joint disorders
  • Patients with bruxism (teeth grinding)
  • Molar teeth without an opposing tooth or fixed prosthetic restoration
  • Molar teeth without adjacent teeth
  • Vital teeth
  • Patients with a history of allergy to the components of the resins

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Prevention

Study locations

Turkey (Türkiye) · 2 centers
  • Mersin University Faculty of Dentistry — Mersin
  • Mersin University — Mersin

Identifiers

NCT: NCT06960070 · 2025/364

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗