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Clinical Trials/NCT03779607
NCT03779607
Unknown
Not Applicable

Clinical Evaluation and Patient Satisfaction Ofshade Matching Between Natural Teeth and Monolithic All-ceramic Crowns Fabricated From Two Materials (Randomized Controlled Clinical Trial)

Cairo University0 sites10 target enrollmentJanuary 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Natural Optical Properties
Sponsor
Cairo University
Enrollment
10
Primary Endpoint
Color match
Last Updated
7 years ago

Overview

Brief Summary

evaluation of color difference between zirconia reinforced lithium silicate (celtra press) VS lithium disilicate (Emax) in relation to natural tooth structure to determine which monolithic material will provide restoration with exact shade and optical properties as natural tooth structure.

Detailed Description

eligible patients will be randomized in 2 equal group between study group (celtra press) and control group (Emax) . Single tooth in esthetic zone requiring full coverage crown is prepared to receive an all ceramic crown of . Grouping: The crowns will be divided into two groups: I:Teeth receiving crowns fabricated from IPS emax press ( ivoclarvivadent) II:Teeth receiving crowns fabricatedfrom Celtrapress(dentsplysirona). Shade will be measured using intraoral spectrophotometer and evaluated. The color 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.

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

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Mohamed el sayed bekhiet

Resident - Fixed prosthodontic department- Faculty of oral and dental medicine

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Age range of the patients from 20-45 years old; able to read and sign the informed consent document, illiterate patient will be avoided.
  • Patients able physically and psychologically to tolerate conventional restorative procedures.
  • Patients with no active periodontal or pulpal diseases, having teeth with good restorations.
  • Patients with teeth problems indicated for full coverage restoration ( coronal fracture where partial coverage would lack retention, malposed or malformed teeth).
  • Patients with root canal treated teeth requiring full coverage restorations with contralatral tooth not filled orfractured.
  • Patients willing to return for follow-up examinations and evaluation.

Exclusion Criteria

  • Patients in the growth stage with partially erupted teeth.
  • Patients with poor oral hygiene and motivation.
  • Pregnant women's to avoid any complication that may occur in dental office due to pregnancy or due to injected anesthetic solution.
  • Patients with psychiatric problems or unrealistic expectation
  • Patients have no opposite occluding dentition in the area intended for restoration\\
  • Patients suffer from parafunctional habits.
  • deep discoloration of abutment .
  • Smokers and heavy caffeine consumers.

Outcomes

Primary Outcomes

Color match

Time Frame: immediately after crown cementation

using USPHS scoring system

Secondary Outcomes

  • Patient satisfaction(immediately after crown cementation)

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