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Clinical Trial Summary

This investigation will be a clinical trial to study the performance of a new resin-based ceramic material for crowns. The material has been approved by the FDA for patient treatment. A computer technique will be used to fabricate the crowns in a single appointment without the need for a temporary crown or second appointment. The purpose of the study is to measure how well the high strength crowns function over an extended period of time.


Clinical Trial Description

The study will be composed of 50 crowns placed in adult patients that have been identified as requiring at least one crown on a posterior tooth. A maximum of two crowns per patient will be completed. All the crowns will be made from the same resilient ceramic CAD/CAM block(Tetric CAD/Ivoclar Vivadent). The crowns are placed using an adhesive bonding process including a total etch process with a universal adhesive (Adhese by Ivoclar Vivadent) and dual-cured resin cement (Variolink Esthetic by Ivoclar Vivadent). The crowns are planned to be evaluated at 6 months, 1 year, 2 years, 3 years, and if funding permits, 4 years, and 5 years. At each appointment, an examination of the crown will be completed as well as clinical photographs, an intraoral digital scan, and impression of the crown. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03716817
Study type Interventional
Source University of Michigan
Contact
Status Active, not recruiting
Phase N/A
Start date October 1, 2018
Completion date October 2026

See also
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Terminated NCT03036579 - Celtra Duo Computer Assisted Design/Computer Assisted Machining (CAD/CAM) Dental Crown Study N/A
Completed NCT03302143 - Radiographic and the Esthetic Outcome of Two Different Bone Grafting Techniques in Early Implant Placement N/A
Recruiting NCT04685161 - Comparison of Surgical Extrusion vs. Fibre Post Restoration for Crown-root Fractured Maxillary Incisors. N/A