Prospective Clinical Trial of Onlay-carrying Patients
-
- STATUS
- Recruiting
-
- 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
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
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
| 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 |
How to participate?
,
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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.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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