NCT05265559

Influence of Operator Factors on Succes and Survival of Indirect Restorations

Status unknown Last updated 3 March 2022

What this trial tests

trial testing Partial Indirect Restoration in Partial Indirect Restoration in 200 participants. Status unknown.

Timeline

9 October 2018

Primary endpoint
1 April 2022

1 July 2025

Quick facts

Lead sponsor	University Medical Center Groningen
Status	Status unknown
Study type	OBSERVATIONAL
Enrollment	200
Start date	9 October 2018
Primary completion	1 April 2022
Estimated completion	1 July 2025
Sites	1 location across Netherlands

Drugs / interventions tested

• Partial Indirect Restoration

Conditions studied

• Partial Indirect Restoration — all drugs for Partial Indirect Restoration →
• Clinical Study — all drugs for Clinical Study →
• Adhesion — all drugs for Adhesion →
• Immediate Dentin Sealing — all drugs for Immediate Dentin Sealing →

Sponsor

University Medical Center Groningen

Who can join

18 and older, any sex, with Partial Indirect Restoration or Clinical Study. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Background: Nowadays, tissue preserving, aesthetically high-quality and sustainable dentistry is more and more becoming the standard way of treatment. To reach those standards, one of the treatment options is applying a partial indirect restoration made by glass ceramics using immediate dental sealing (IDS). Using IDS, a protocol is followed to applicate a dentin bonding agent to freshly cut dentin when it is exposed during tooth preparation for indirect restorations (inlays/onlays, crowns). The preparation made for partial restorations is minimal invasive. Glass ceramic restorations have very high survival rates (90 to 100% after five years) (Morimoto et al., 2016) and glass ceramic mimics the color and structure of the tooth very well.

This kind of treatment is gaining interest and increasingly applied however little information is available on the long-term effects when multiple general practitioners apply these restorations.

Objectives: The main goal of this study is to evaluate partial posterior ceramic restorations with the application of an immediate dentin sealing (IDS) performed by various practitioners.

Study design and population:

Twenty dental practitioners, who followed a course on making ceramic partial restorations using IDS, will be asked to include patients for this study. The dental practitioners are being asked to share their data (occlusal light photo's, impression and x-rays) of twenty-five restorations they make after having the course. Restorations of individuals with a minimum age of 18 will be included. The information from pictures and impressions will be evaluated.

Items to evaluate

The practitioners will be interviewed to get to know in what circumstances they do their treatment. Items that are discussed are:

* using rubber dam;
* using magnification by means of loupes/microscope;
* scheduled time for the treatment;
* number of restorations after following the course.

Initial data (gathered directly after treatment) will be evaluated looking at:

* surface of preparation after IDS;
* size of the prepared surface;
* color.

Follow up data will be evaluated looking at:

* tooth extraction
* fracture restoration
* fracture tooth
* secondairy caries
* de-bonding
* endodontic problems

Outcome: Failures (fracture, de-bonding, secondairy cariës, endodontic problems) are the main outcome measurements.

Description and estimation of the load and risk for the subjects:

No extra intervention is performed. The dental practitioners will provide their data (i.e. impressions, occlusal light photo's) and these will be evaluated by the researchers. Follow up data will be gathered from X-rays already made for periodical oral examination (taking the caries risk into account). Summarizing, there is no extra load or risk for the patients.

Studie design Prospective practice-based research, multicenter.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.