Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06960070

Clinical Success of Onlays Fabricated With Different Types of Resin

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.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–84 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Mersin University, Mersin, Turkey (Türkiye)

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Saremco print resin

Device

The teeth were restored with Saremco print resin via Asiga Max printer according to the manufacturer's instructions.

Varseosmile Crownplus resin

Device

The teeth were restored with Varseosmile Crownplus resin via Asiga Max printer according to the manufacturer's instructions.

Varseosmile TriniQ resin

Device

The teeth were restored with Varseosmile TriniQ resin via Asiga MAx printer according to the manufacturer' instructions

Primary outcomes

  1. Clinical performance

    Time frame: Baseline- 6 months-12 months

    The clinical evaluation of restorations bonded to teeth will be performed at baseline, at 6 months, and at 12 months using the World Dental Federation (FDI) criteria which are divided into 3 main categories as functional, biological and esthetic properties. Each property is typically scored on a 1 to 5 scale:

    • - Clinically excellent
    • - Clinically good
    • - Clinically sufficient
    • - Clinically insufficient
    • - Clinically poor

Study contacts

Contact information is provided by the study sponsor or research team.

Esra Cengiz Yanardag, DDS, PhD

CONTACT

[email protected]

+905052443472

Sponsors and collaborators

Lead sponsor

Mersin University

Other

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
May 7, 2025
Registry last updated
Sep 10, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.