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Clinical Trials/NCT03521024
NCT03521024
Unknown
Not Applicable

Evaluation of Esthetic and Biomechanical Outcome of Maxillary Anterior Single-Tooth Zirconia Implant Supported PEKK Crowns Versus Lithium Disilicate Crowns on PEKK Abutments: Randomized Controlled Trial

Cairo University0 sites10 target enrollmentSeptember 15, 2018
ConditionsTooth Loss

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Tooth Loss
Sponsor
Cairo University
Enrollment
10
Primary Endpoint
Esthetic outcome
Last Updated
7 years ago

Overview

Brief Summary

aim of study is to evaluate esthetic and biomechanical outcome of maxillary anterior single-tooth zirconia implant supported PEKK crowns compared to lithium disilicate crowns on PEKK abutments .

Detailed Description

High performance polymers may be a valid alternative to other conventional materials for abutments and crowns over zirconia implants because of their cushioning effect and elastic modulus (5.1GPa), which absorb occlusal forces and avoid overload of the underlying bone from the direct transmission of biting impacts ; which could optimize and preserve osseointegration with time. Zirconia implants with high performance polymers restorations can be considered a good alternative for replacing natural teeth. For many years lithium disilicate has been the esthetics standard used in Veneers ,Inlays , onlays, occlusal veneers, partial crowns,minimally invasive crowns and Implant superstructures due to its natural-looking tooth colouring and excellent light-optical properties. Due to the promising esthetics of high performance polymers as it can be veneered with different veneering materials it would successfully restore esthetics.

Registry
clinicaltrials.gov
Start Date
September 15, 2018
End Date
September 15, 2019
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Lamiaa Said Zaki AbdelSalam Elfadaly

Dr.

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Age \>18 years
  • No active intraoral or systemic disease
  • No pregnancy or lactation
  • controlled periodontal conditions
  • Adequate bone volume to place an implant
  • Occlusal function with a natural tooth

Exclusion Criteria

  • Current pregnancy.
  • Psychiatric disorders.
  • Poor motivation.
  • Several occlusal parafunction.
  • Persistent intraoral infections.
  • Severe mucosal disease.
  • Active periodontitis.
  • Poor oral hygiene.
  • Lack of occluding dentition at implant rehabilitation level

Outcomes

Primary Outcomes

Esthetic outcome

Time Frame: 9 month

measured by pink and white esthetics score

Secondary Outcomes

  • bone resorption(9 month)

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