Clinical Performance Clinical Trial
Official title:
Prospective Clinical Trial of Onlay-carrying Patients
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).
Status | Recruiting |
Enrollment | 300 |
Est. completion date | January 1, 2025 |
Est. primary completion date | January 1, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
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. |
Country | Name | City | State |
---|---|---|---|
Spain | Lucia Fernandez-Estevan | Valencia |
Lead Sponsor | Collaborator |
---|---|
University of Valencia |
Spain,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Clinical behaviour | Analyze clinical behavior taking into account possible variables that may influence using modified UPSHS criteria | Through study completion, an average of 5 years. | |
Primary | Survival | Analyze the survival over time of this type of treatment | Through study completion, an average of 5 years. | |
Secondary | Complications | Analyze complications over time of this type of treatment using modified UPSHS criteria | Through study completion, an average of 5 years. |
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