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Not yet recruiting NCT07051590

Adjustment Period for Partial Crowns

No phase Interventional Deep Caries Lesion of Pemanent 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: cad cam, 3D printer.
Who it may be relevant to
Registry conditions: Deep Caries Lesion of Pemanent Teeth. Basic parameters: 18 years — 65 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

Evaluation of the Time Required for Clinical Adaptation of Partial Dentures Based on Additive and Subtractive Manufacturing: A Randomized Controlled Clinical Study

Overview

The aim of this study is to compare the occlusal accuracy of CAD/CAM milled and 3D printed crowns guided by an occlusal device, starting from the same digital CAD design.

Detailed description

The subject of this study is to compare the occlusal closure performance of onlay restorations produced from CAD-CAM blocks and onlay restorations produced using 3D printer technology. The Occlusense device has the capacity to measure occlusal contact points and force distribution through digital pressure sensors, providing accurate data in clinical research.

This study is a randomized clinical trial conducted using a split-mouth design. Onlay restorations produced using different manufacturing methods will be applied to two teeth of the same patient, and the occlusal closures of both restorations will be evaluated.

Interventions

  • Device cad cam
    Occlusion assessment in CAD CAM restorations
  • Device 3D printer
    Crowns produced with 3D technology

Primary outcome measures

  • crown adjustment times [Time frame: 1-6 month]

Eligibility criteria

Inclusion criteria

  • Devitalized and vital teeth with tubercle loss
  • ASA I

Exclusion criteria

  • Teeth with periapical lesions
  • Temporomandibular joint disorder or bruxism
  • Periodontal disease
  • Symptomatic vital teeth

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
Treatment

Study locations

Turkey (Türkiye) · 1 center
  • Çukurova Üniversitesi — Adana

Publications

  • Lee WS, Lee DH, Lee KB. Evaluation of internal fit of interim crown fabricated with CAD/CAM milling and 3D printing system. J Adv Prosthodont. 2017 Aug;9(4):265-270. doi: 10.4047/jap.2017.9.4.265. Epub 2017 Aug 16. PMID 28874993

Identifiers

NCT: NCT07051590 · restorative dentistry

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗