Prospective Clinical Trial of Onlay-carrying Patients
-
- STATUS
- Recruiting
-
- days left to enroll
- 10
-
- participants needed
- 300
-
- sponsor
- University of Valencia
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).
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.
Details
| Condition | Survival Rate, Clinical Performance, Success |
|---|---|
| Age | 18years - 100years |
| Treatment | Partial restoration in posterior teeth |
| Clinical Study Identifier | NCT04396080 |
| Sponsor | University of Valencia |
| Last Modified on | 19 February 2024 |
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
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