Adjustment Period for Partial Crowns

NCT ID: NCT07051590

Last Updated: 2025-07-04

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

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-08-20

Study Completion Date

2027-01-20

Brief Summary

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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

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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.

Conditions

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Deep Caries Lesion of Pemanent Teeth

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

The subject of this study is to compare the occlusal closure performance of onlay restorations produced from CAD-CAM blocks with 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
Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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additive

manufactured with 3D

Group Type EXPERIMENTAL

3D printer

Intervention Type DEVICE

Crowns produced with 3D technology

subtractive

manufactured with CAD/CAM

Group Type EXPERIMENTAL

cad cam

Intervention Type DEVICE

Occlusion assessment in CAD CAM restorations

Interventions

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cad cam

Occlusion assessment in CAD CAM restorations

Intervention Type DEVICE

3D printer

Crowns produced with 3D technology

Intervention Type DEVICE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ceren Sire

OTHER

Sponsor Role lead

Responsible Party

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Ceren Sire

research assistant

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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zeliha g bek kürklü, doçent

Role: STUDY_DIRECTOR

çukurova üniversitesi diş hekimliği restoratif diş tedavisi

Doç. Dr. Dt

Role: STUDY_DIRECTOR

çukurova üniversitesi diş hekimliği restoratif diş tedavisi

Locations

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Çukurova Üniversitesi

Adana, Sarıçam, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Central Contacts

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ceren şire, araştırma görevlisi diş hekimi

Role: CONTACT

+905335103035 ext. 05335103035

zeliha g bek kurklu, doçent

Role: CONTACT

+9005334500892

References

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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.

Reference Type RESULT
PMID: 28874993 (View on PubMed)

Other Identifiers

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restorative dentistry

Identifier Type: -

Identifier Source: org_study_id

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