← Eichor
Study identifier: NCT07031856 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Comparison of Clinical Performance of Partial Restorations Fabricated With Three-Dimensional Printer and CAD-CAM

Condition: Dental Caries · Dental Restoration, Permanent · Tooth Diseases  ·  Sponsor: Cukurova University

PhaseNA
Planned participants12
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersYes

About this study

The aim of this clinical study is to compare CAD-CAM and 3D restorations in individuals with two hard tissue losses or restorations in their mouths. The main question it aims to answer is: Is there a difference between CAD-CAM and 3D restorations according to FDI criteria? Researchers will compare participants to see if there is a difference between the two restorations according to FDI criteria. In this split-mouth study, participants will be randomized to receive a CAD-CAM partial restoration on one tooth and a 3D partial restoration on the other tooth.

This description comes directly from the study's public registry record.

Talk to the study team

Research Assistant  ·  +90 0544 745 8633  ·  yarenncoskun@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Çukurova Üniversitesi Diş Hekimliği FakültesiAdana, Sarıçam, Turkey (Türkiye)Recruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07031856