The Restoration of Endodontically Treated Teeth Using Indirect Full Coverage Restorations Compared to Direct Composite Resin Restorations
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- STATUS
- Recruiting
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- participants needed
- 60
-
- sponsor
- University of Jordan
Summary
The use of full cuspal coverage restoration for the management root treated teeth was
advocated by many clinical studies and supported by systematic reviews. However, most of the
studies did not take into account the amount of tooth structure remaining before providing
cuspal coverage. The strength and
The aims of this randomized clinical trial is to compare the survival and success of root
treated teeth with occlusal
Description
The management of posterior endodontically treated teeth (ETT) is still to this day
considered a controversial topic.The use of full cuspal coverage restoration for the
management ETT was advocated by many clinical studies and supported by systematic reviews.
However, most of the studies did not take into account the amount of tooth structure
remaining before providing cuspal coverage. An ETT tooth with an MOD
The aims of this randomized clinical trial is to compare the survival and success of ETT with
occlusal
The groups are:
Group 1: Managed with direct intracoronal composite resin restoration. Group 2: Managed with a direct composite resin restoration, followed by an indirect full coverage restoration.
Patients will be recalled at 1 year, 3 years and 5 years.
Group 2: Patients receiving a composite resin restoration and followed with an indirect full coverage restoration.
The same steps used as for group 1 would be followed to build the composite resin core. This
will be followed with a preparation for the indirect full cuspal restoration. Three
additional silicone putty indices will be made; one will be made for the production of a
- include
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- Supra or equigingival margins if aesthetic was of concern.
- Chamfer finish-line
- 2 mm occlusal reduction;
- 1.5 mm axial reduction all around Following the application of two double retraction cord sizes 00 and 0 (Ultradent), the impression will be made with additional silicone (Zermack) and the cast poured in Die stone. The crown will be fabricated in the laboratory.
The
Follow-up appointments and data Collection
Clinical evaluation will include:
Visual inspection conducted with loops at magnification 4.5- Examination of the continuity of the margins of the restoration with the tooth structure by use of an explorer
- Periodontal probing performed with a periodontal probe.
- Color photos (1:1 mirror shots) of the restorations were taken with standard film
- Periapical and bitewing
radiographic examination was performed by use of a paralleling technique at 65 kV and 8 mA. - Patients reported outcome measures (PROM)
Evaluation of success or failure will be performed by 2 examiners other than the operator.
Details
Condition | Tooth, Nonvital |
---|---|
Age | 18years - 100years |
Treatment | Direct composite resin restoration, Direct composite resin restoration followed by full coverage metal ceramic crown |
Clinical Study Identifier | NCT04249726 |
Sponsor | University of Jordan |
Last Modified on | 19 February 2024 |
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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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