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Clinical Trials/NCT04320758
NCT04320758
Unknown
Not Applicable

One Year Clinical Evaluation of Translucent Zirconia Crowns in Dental Esthetic Zone With Biologically Oriented Preparation Technique (BOPT) Versus Conventional Preparation (Randomized Clinical Trial)

Cairo University1 site in 1 country22 target enrollmentOctober 30, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Single Crowns in Aesthetic Dental Zone
Sponsor
Cairo University
Enrollment
22
Locations
1
Primary Endpoint
Marginal adaptation
Last Updated
5 years ago

Overview

Brief Summary

Aim of the studyto evaluate the clinical behavior of translucent zirconia crown in dental esthetic zone with biologically oriented preparation technique versus conventional preparation.

Registry
clinicaltrials.gov
Start Date
October 30, 2020
End Date
December 30, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Kareem Talaat Abdelwahab Ahmed Ali

Resident,Fixed Prosthodontics Department,Faculty of Dentistry

Cairo University

Eligibility Criteria

Inclusion Criteria

  • All subjects are required to be:
  • From 21-35 years old, be able to read and sign the informed consent document.
  • Have no active periodontal or pulpal diseases, have teeth with good restorations
  • Psychologically and physically able to withstand conventional dental procedures
  • Patients with teeth problems indicated for single all ceramic restoration in maxillary esthetic zone cr
  • Badly decayed teeth
  • Teeth restored with large filling restorations
  • Endodontically treated teeth
  • Malformed teeth
  • Malposed teeth (Tilted, over-erupted, rotated, etc.)

Exclusion Criteria

  • Patient less than 21or more than 35 years
  • Patient with active resistant periodontal diseases
  • Patients with poor oral hygiene and uncooperative patients
  • Pregnant women
  • Patients in the growth stage with partially erupted teeth
  • Psychiatric problems or unrealistic expectations
  • Patient with periodontal problems
  • patients with malocclusion or parafunctional habits

Outcomes

Primary Outcomes

Marginal adaptation

Time Frame: 1 year

Measured using Modified USPHS criteria1

Study Sites (1)

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