NCT07051590

Brief Summary

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.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
8mo left

Started Aug 2025

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress51%
Aug 2025Jan 2027

First Submitted

Initial submission to the registry

June 3, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

July 4, 2025

Completed
2 months until next milestone

Study Start

First participant enrolled

August 20, 2025

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 20, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

January 20, 2027

Last Updated

July 4, 2025

Status Verified

July 1, 2025

Enrollment Period

1.3 years

First QC Date

June 3, 2025

Last Update Submit

July 3, 2025

Conditions

Keywords

3Docclusensepartial crowncad/cam

Outcome Measures

Primary Outcomes (1)

  • crown adjustment times

    Using the occlusal relationships recorded with the occlusense recorder prior to the restoration preparation as a guide, the occlusal contacts will be adjusted at maximum intercuspation (ICM) and during protrusive and lateral excursive movements. The duration of these adjustments will be measured.

    1-6 month

Study Arms (2)

additive

EXPERIMENTAL

manufactured with 3D

Device: 3D printer

subtractive

EXPERIMENTAL

manufactured with CAD/CAM

Device: cad cam

Interventions

cad camDEVICE

Occlusion assessment in CAD CAM restorations

subtractive

Crowns produced with 3D technology

additive

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Devitalized and vital teeth with tubercle loss
  • ASA I

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Çukurova Üniversitesi

Adana, Sarıçam, 01250, Turkey (Türkiye)

Location

Related Publications (1)

  • 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.

Study Officials

  • zeliha g bek kürklü, doçent

    çukurova üniversitesi diş hekimliği restoratif diş tedavisi

    STUDY DIRECTOR
  • Doç. Dr. Dt

    çukurova üniversitesi diş hekimliği restoratif diş tedavisi

    STUDY DIRECTOR

Central Study Contacts

ceren şire, araştırma görevlisi diş hekimi

CONTACT

zeliha g bek kurklu, doçent

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: 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
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
research assistant

Study Record Dates

First Submitted

June 3, 2025

First Posted

July 4, 2025

Study Start

August 20, 2025

Primary Completion (Estimated)

December 20, 2026

Study Completion (Estimated)

January 20, 2027

Last Updated

July 4, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share

Locations