Prospective Clinical Trial of Onlay-carrying Patients

Not Applicable

Recruiting

• Conditions: Survival Rate; Clinical Performance; Success
• Interventions: Procedure: Partial restoration in posterior teeth

• Registration Number: NCT04396080
• Lead Sponsor: University of Valencia

Brief Summary

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).

Detailed 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.

Study Timeline

• Study Start: 2019-01-01
• Status Verified: 2020-03
• Study First Submitted: 2020-05-11
• Study First Submitted QC: 2020-05-15
• Last Update Submitted: 2020-05-15
• Study First Posted: 2020-05-20
• Last Update Posted: 2020-05-20
• Primary Completion: 2024-01-01
• Study Completion: 2025-01-01

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 300

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 & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Onlays behaviour depending on materials	Partial restoration in posterior teeth	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.

Primary Outcome Measures

Name	Time	Method
Survival	Through study completion, an average of 5 years.	Analyze the survival over time of this type of treatment

Secondary Outcome Measures

Name	Time	Method
Complications	Through study completion, an average of 5 years.	Analyze complications over time of this type of treatment using modified UPSHS criteria

Trial Locations

Locations (1)

Lucia Fernandez-Estevan; 🇪🇸 Valencia, Spain