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Clinical Trials/NCT06539546
NCT06539546
Not yet recruiting
Not Applicable

Shade Matching and Patient Satisfaction of Yttria Stabilized Multilayered Zirconia and Lithium Disilicate Restorations: a Randomized Controlled Clinical Trial

Cairo University0 sites22 target enrollmentSeptember 1, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Mutilated Teeth
Sponsor
Cairo University
Enrollment
22
Primary Endpoint
Color difference
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

The aim of the study is to determine whether Yttria stabilized multilayered zirconia restorations will differ from lithium disilicate restorations in shade matching and patient satisfaction in patients requiring full coverage restorations.

Detailed Description

Steps in short: Single tooth in the esthetic zone requiring full coverage crown is prepared to receive an all-ceramic crown, The restorations will be divided into two groups: I: Teeth receiving restorations fabricated from Lithium disilicate II: Teeth receiving restorations fabricated from yttria stabilized multilayered zirconia. Shade will be measured using intraoral spectrophotometer and evaluated. The colour difference (ΔE) will be calculated for each sample using the following equation: ΔE =\[(ΔL) ²+(Δa) ² + (Δb) ²\] ½, ΔE (perceptibility threshold) will be evaluated for each group. Participant timeline the patient will be treated in visits designated as follows: Visit 1: Preoperative records, face-to-face adherence reminder session, clinical, radiographic for examination, intraoral photographs and primary impression (Alginate impression) diagnostic cast construction. Visit 2: teeth preparation and secondary impression using addition silicone rubber base material and temporary restoration. Visit 3: placement and permanent cementation of the final restoration using resin cement.

Registry
clinicaltrials.gov
Start Date
September 1, 2024
End Date
September 1, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Yasmin Mohamed

Principal Investigator

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Patients in the growth stage with partially erupted teeth.
  • Patients with poor oral hygiene and motivation.
  • Patients with psychiatric problems or unrealistic expectations (patient that has phobia from dental treatments or needle bunch).
  • Patients suffer from parafunctional habits.

Outcomes

Primary Outcomes

Color difference

Time Frame: immediate after cementation

By Intraoral Spectrophotometer, color difference between the restoration and the adjacent or contralateral natural tooth will be measured by the unit (ΔE), (ΔE) will be measured for each sample.

Secondary Outcomes

  • Patient satisfaction(immediate after cementation)

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