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Completed

NCT Number: NCT04054674

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

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

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Key information

Age range

20 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cairo university

Cairo, Egypt

About this study

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

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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)

Treatment and study plan

Abutments with flat occlusal scheme preparation restored by lithium disilicate crowns

Procedure

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.

Primary outcomes

  1. Measuring number of Fracture

    Time frame: one year

    using USPHS criteria for clinical evaluation

Secondary outcomes

  1. Degree of Marginal adaptation

    Time frame: one year

    using USPHS criteria for clinical evaluation

  2. Degree of Marginal discoloration

    Time frame: one year

    using USPHS criteria for clinical evaluation

  3. Presence of Caries

    Time frame: one year

    using USPHS criteria for clinical evaluation

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Aug 13, 2019
Registry last updated
Apr 15, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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