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Clinical Performance Of Lithium Disilicate Crowns Restoring Endodontically Treated Teeth With Two Occlusal Preparation Schemes

Clinical Performance Of Lithium Disilicate Crowns Restoring Endodontically Treated Teeth With Two Occlusal Preparation Schemes

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04054674
Enrollment
40
Registered
2019-08-13
Start date
2019-10-10
Completion date
2021-10-10
Last updated
2022-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fracture of Lithium Disilicate (e.Max) Crowns

Keywords

e.max, occlusal scheme, endodontically treated teeth

Brief summary

The aim of this study is to evaluate the clinical performance of lithium disilicate crowns restoring endodontically treated teeth with two occlusal preparation schemes.

Detailed description

Statement of the problem: The endodontically treated teeth need to be restored back to form, function and aesthetics. The quality of the coronal restoration will directly impact on their survival and success. The aim of the coronal restoration of endodontically treated teeth is to provide the necessary strength for the restoration/tooth complex through tooth preparation in order to withstand functional stress and prevent crown and/or root fracture. The use of ceramic crowns has increased substantially in recent years because of their superior esthetics and high mechanical properties. Long term success of all ceramic crowns is affected by many factors and the failure patterns of these all ceramic crowns should be inspected closely to detect their clinical performance. Rationale for carrying out the trial: Endodontic treatment weakens posterior teeth and ought to be covered by crowns.The capability of these crowns to bear load relies on the preparation of an appropriate design and the selection of a crown material with adequate fracture strength and thickness. In vital teeth, the anatomic occlusal preparation design is followed such that the occlusal surface is reduced uniformly, maintaining the cusps and normal inclined planes but at a reduced height. This aids in minimizing the risk of pulp injury. In contrast, in non-vital teeth, this design can be modified such that the occlusal surface is prepared in two planes (buccal and lingual planes). A flat prepared occlusal surface provides less quantitative and better qualitative stresses when compared to an anatomically prepared surface

Interventions

PROCEDUREAbutments with flat occlusal scheme preparation restored by lithium disilicate crowns

Clinical trials lacks information about flat occlusal preparation design in case of endodontically treated teeth. Therefore, this is tested during preparation when compared to planer occlusal preparation while the final restoration in both arms is lithium disilicate (e.max) crowns.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Have no active periodontal diseases or periapical pathosis * No tooth mobility or furcation involvement with sufficient occluso-gingival height * Psychologically and physically able to withstand conventional dental procedures * Patients with good endodontically treated teeth indicated for full coverage restorations * Able to return for follow-up examination and evaluation

Exclusion criteria

* Patient with active resistant periodontal diseases * Patients with poor oral hygiene and uncooperative * Pregnant women that won't be able to come for follow-up visits * Patients in the growth stage with partially erupted teeth * Psychiatric problems or unrealistic expectations * Lack of opposing dentition in the area of interest * Patients with poor root canal treatment * Patients with parafunctional habits (eg. Bruxism)

Design outcomes

Primary

MeasureTime frameDescription
Measuring number of Fractureone yearusing USPHS criteria for clinical evaluation

Secondary

MeasureTime frameDescription
Degree of Marginal adaptationone yearusing USPHS criteria for clinical evaluation
Degree of Marginal discolorationone yearusing USPHS criteria for clinical evaluation
Presence of Cariesone yearusing USPHS criteria for clinical evaluation

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026