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Clinical Trials/NCT04320758
NCT04320758UnknownNot 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 University2 sites in 1 country22 target enrollmentStarted: October 30, 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
22
Locations
2
Primary Endpoint
Marginal adaptation

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
21 Years to 35 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

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.)
  • Spacing between maxillary teeth in esthetic zone
  • Able to return for follow-up examinations and evaluation

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

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Kareem Talaat Abdelwahab Ahmed Ali

Resident,Fixed Prosthodontics Department,Faculty of Dentistry

Cairo University

Study Sites (2)

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