Clinical Trials Directory

Trials / Completed

CompletedNCT05346744

Occlusal Contact Trueness Affected by Six Chairside CAD/CAM Ceramic Materials

Quantitative Clinical Evaluation of the Occlusal Contact Trueness Affected by Six Chairside CAD/CAM Ceramic Materials:a Self-control Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
10 (actual)
Sponsor
Fujian Medical University · Academic / Other
Sex
All
Age
20 Years – 30 Years
Healthy volunteers
Accepted

Summary

The aim of this clinic self-control study was to evaluate the trueness of occlusal contact affected by six ceramic materials during chairside fabricating process and offer recommendations for occlusal offset according to different ceramic materials in CEREC CAD/CAM design process.

Detailed description

Ten participants were selected for this study. InCoris TZl(ZIR), Celtra Duo(CD), IPS e.max(EMA), UPCERA LICI (LC), Vita enamic(ENA), UPCERA RUNCI (RC) were used to produce crowns for everyone by CEREC chairside CAD/CAM system. The milling trueness, postprocessing trueness and clinical adjustment of occlusal contact were quantitatively analyzed by the ATOS high-precision scanner and Geomagic reverse engineering software.

Conditions

Interventions

TypeNameDescription
OTHERChairside CAD/CAM ceramic materials for dental restoration6 crowns made from 6 chairside ceramic materials were milled by CEREC MCXL-EF mode for mandibular first molar of each participant. The six materials are as follows: ZIR: InCoris TZI (Dentsply Sirona, York, PA), CD: Celtra Duo (Dentsply Sirona, York, PA), EMA: e.max CAD (ivoclar, Vivadent AG), LC: LiCi (UPCERA, China), ENA: Vita Enamic (Vita Zahnfabrik, Bad Sackingen, Germany) RC: RunCi (UPCERA, China)

Timeline

Start date
2019-11-01
Primary completion
2021-07-01
Completion
2021-08-01
First posted
2022-04-26
Last updated
2022-04-26

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05346744. Inclusion in this directory is not an endorsement.