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Clinical Trials/NCT03697018
NCT03697018
Unknown
Not Applicable

Evaluation of Antagonist Wear Behavior and Patient Satisfaction of Monolithic Zirconia Versus Lithium Silicate Zirconia Crowns

Cairo University0 sites26 target enrollmentOctober 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Wear of the Natural Enamel
Sponsor
Cairo University
Enrollment
26
Primary Endpoint
wear of the antagonist natural enamel
Last Updated
7 years ago

Overview

Brief Summary

evaluation of wear behavior and patient satisfaction of monolithic zirconia and zirconia reinforced glass crowns after follow-up periods 0,3,6,12 months.

Detailed Description

two groups of patients will be selected according to special inclusion criteria n=13 in each group total of 26. each group will receive one of the crowns used in this study either ( monolithic zirconia or zirconia reinforced lithium silicate glass) after crown delivery wear and patient satisfaction will be recorded at 0,3,6,12 moths follow-up periods.

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

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Esraa Mohamed Hany

PHD candidate, fixed prosthodontic department, faculty of Oral and dental Medicine

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Patient age range from 20-60 to be able to read and write in order to sign the informed consent document.
  • Patients physically and psychologically able to tolerate conventional restorative procedures.
  • Patients with no active periodontal and or pulpal diseases, having teeth with good restorations.
  • Patients with root canal treated teeth requiring full coverage restorations.
  • Patients indicated for full coverage (e.g. moderate to severe discoloration, coronal fracture, malposed or malformed teeth).
  • Patients willing to return for follow-up examinations and assessments

Exclusion Criteria

  • Patients in the growth stage with partially erupted teeth.
  • Patient with poor oral hygiene.
  • Patients with psychiatric problems or unrealistic expectations
  • Patient with no opposite occluding dentition in the area intended for restoration.
  • Patient suffering from Para functional habits.

Outcomes

Primary Outcomes

wear of the antagonist natural enamel

Time Frame: from baseline till one year

loss of opposing tooth structure which will be measured by 3D Profilometer

Secondary Outcomes

  • patient satisfaction(from baseline till one year)

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