Clinical Performance, Success, Survival Rate
Conditions
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.
Interventions
PROCEDUREPartial 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.
Sponsors
University of Valencia
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
Patients who require it, will be treated with posterior partial restorations. That will be the intervention.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
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.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Survival | Through study completion, an average of 5 years. | Analyze the survival over time of this type of treatment |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Complications | Through study completion, an average of 5 years. | Analyze complications over time of this type of treatment using modified UPSHS criteria |
Other
| Measure | Time frame | Description |
|---|---|---|
| Clinical behaviour | Through study completion, an average of 5 years. | Analyze clinical behavior taking into account possible variables that may influence using modified UPSHS criteria |
Countries
Spain
Contacts
Primary ContactNaia Bustamante Hernández, Máster
Outcome results
None listed