Prospective Clinical Trial of Onlay-carrying Patients

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

Clinical Phase

NA

Total Enrollment

300 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-01-01

Study Completion Date

2025-01-01

Brief Summary

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A record of the type of onlay will be made with respect to its extension, tooth or teeth to be treated, the material of clothing and the substrate on which the adhesion and cementing method, as well as the type of antagonist. To complete it, a complete clinical oral examination will be performed with oral mirrors, examination probes, joint paper, disposable gloves, masks, paper napkins, plastic cups, dental equipment lighting lamp, cold spray , photogrammed camera, including an intraoral scan to have a 3D file of the patient's condition on the day of embedding placement.

Once treatment is complete, the patient should go to routine check-ups in which a full intraoral exploration and data collection intended to be carried out analyze the following variables (USPHS modificated): possible decemented and fractured, decay and marginal integrity, sensitivity or loss of vitality, as well as the degree of patient satisfaction (VAS).

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Detailed Description

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The same intervention will be carried out during the duration of the project, collecting the variables:

* baseline recall. (cementing day)
* 1 month.
* 6 months.
* annually.

Conditions

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Success Survival Rate Clinical Performance

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Patients who require it, will be treated with posterior partial restorations. That will be the intervention.

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Onlays behaviour depending on materials

Patients who require it as treatment option will be treated with posterior partial restorations, and will have clinical follow-up to obtain a comparison of the behavior of subsequent restorations based on the material.

Group Type EXPERIMENTAL

Partial restoration in posterior teeth

Intervention Type PROCEDURE

Teeth in need of onlays that will be treated with this type of treatment, choosing the most suitable material for each patient and following the manufacturer's instructions for their cementing and adhesion.

Interventions

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Partial restoration in posterior teeth

Teeth in need of onlays that will be treated with this type of treatment, choosing the most suitable material for each patient and following the manufacturer's instructions for their cementing and adhesion.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Healthy adult patients (ASA I) susceptible to treatment with onlays in the posterior region treated at the University Dental Clinic (Master's Clinic in Dental Prosthetics of the Department of Stomatology of the Faculty of Medicine and dentistry)