Prospective Clinical Trial of Onlay-carrying Patients

University of Valencia

Status: Enrolling

Conditions: Clinical Performance; Success; Survival Rate

Treatments: Procedure: Partial restoration in posterior teeth

Study type: Interventional

Funder types: Other

Identifiers

NCT04396080

H1543943843337

Details and patient eligibility

About

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).

Full 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.

Enrollment: 300 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

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.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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300 participants in 1 patient group

Onlays behaviour depending on materials

Experimental group

Description:

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.

Treatment:

Procedure: Partial restoration in posterior teeth