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Prospective Clinical Trial of Onlay-carrying Patients

Prospective Clinical Trial of Onlay-carrying Patients

Recruiting
18 years and older
All
Phase N/A

Overview

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).

Description

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.

Eligibility

Inclusion Criteria:

  • 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)

Exclusion Criteria:

  • Minor patients.
  • Medically committed patients.
  • Patients with active cavities.
  • Patients with active periodontal disease.

Study details
    Survival Rate
    Clinical Performance
    Success

NCT04396080

University of Valencia

5 August 2020

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