Influence of Operator Factors on Succes and Survival of Indirect Restorations

NCT ID: NCT05265559

Last Updated: 2022-03-03

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

UNKNOWN

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-10-09

Study Completion Date

2025-07-01

Brief Summary

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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 cariƫs, 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.

Detailed Description

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Conditions

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Partial Indirect Restoration Clinical Study Adhesion Immediate Dentin Sealing Posterior Region Operator Factors

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Partial Indirect Restoration

Dental restorative treatment

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Healthy individuals
* Adults

Exclusion Criteria

* Periodontal unstable situation
* Endodontic unstable situation
* Allergies for one or more of the used products
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University Medical Center Groningen

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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University Medical Center Groningen

Groningen, , Netherlands

Site Status RECRUITING

Countries

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Netherlands

Central Contacts

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M.M.M. Gresnigt, M.D.

Role: CONTACT

+31647494611

Facility Contacts

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M.M.M. Gresnigt, M.D.

Role: primary

Other Identifiers

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201800678

Identifier Type: -

Identifier Source: org_study_id

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