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

NCT ID: NCT07031856

Last Updated: 2025-06-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

12 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-07-31

Study Completion Date

2026-11-30

Brief Summary

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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.

Detailed Description

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Conditions

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Dental Caries Dental Restoration, Permanent Tooth Diseases

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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3D printer partial crown

Participant with restoration produced with 3D printer

Group Type EXPERIMENTAL

3D printer partial crown

Intervention Type OTHER

Comprasion of partial restorations made with 3D printer

Cad-Cam partial crown

Participant with restoration produced with Cad-Cam

Group Type OTHER

Treatment as usual

Intervention Type OTHER

Cad-cam printer partial crown

Interventions

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3D printer partial crown

Comprasion of partial restorations made with 3D printer

Intervention Type OTHER

Treatment as usual

Cad-cam printer partial crown

Intervention Type OTHER

Eligibility Criteria

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Exclusion Criteria

Patients with systemic conditions that may affect the study process (e.g. diabetes, autoimmune diseases).

* Patients with excessive bruxism or parafunctional habits.
* Pregnant or lactating women.
* Patients with gum disease or severe bone loss.
* Patients with a history of allergic reactions.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Cukurova University

OTHER

Sponsor Role lead

Responsible Party

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Yaren Cosgun

Research Assistant

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

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Research Assistant

Role: CONTACT

+90 0544 745 8633

Other Identifiers

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T.C. Ç.Ü BAP

Identifier Type: -

Identifier Source: org_study_id

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