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Clinical Trials/NCT04738513
NCT04738513
Unknown
Not Applicable

One Year Clinical Evaluation of New Gradient Technology Monolithic Zirconia (5Y-TZP/3Y-TZP) Crowns in Dental Esthetic Zone With Vertical Versus Conventional Preparation Techniques (Randomized Clinical Trial)

Cairo University1 site in 1 country40 target enrollmentMarch 1, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Single Anterior Crowns
Sponsor
Cairo University
Enrollment
40
Locations
1
Primary Endpoint
Marginal integrity
Last Updated
5 years ago

Overview

Brief Summary

The aim of this study is to evaluate the clinical behavior of zirconia crowns in dental esthetic zone with vertical versus conventional preparation techniques using a new gradient technology monolithic zirconia (5Y-TZP/3Y-TZP).

Detailed Description

Introduction: A good relationship between dental restorations and the periodontium is one of the most important aspects to ensure clinical success both in terms of esthetics and function. Dental preparation for fixed prostheses can take various forms classified as horizontal preparation with a defined margin (chamfer), or vertical, or without a margin/finish line. According to some clinical reports, vertical preparation technique provides an increases in the gingival thickness and a greater stability of the gingival margin. Moreover, vertical preparation is characterized by being more conservative with tooth structure. Also, taking impressions is easier since it is a finish area and not a defined line. Null hypothesis: 1. There will be no difference between vertical and conventional preparations in the clinical behavior of zirconia crowns in dental esthetic zone at baseline,3,6,9,12 months evaluation. 2. There will be no difference between vertical and conventional preparations in the patient satisfaction of zirconia crowns in dental esthetic zone at baseline,3,6,9,12 months evaluation.

Registry
clinicaltrials.gov
Start Date
March 1, 2021
End Date
July 1, 2022
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Mennatalla Ahmed Emad ElGendy

Principal investigator

Cairo University

Eligibility Criteria

Inclusion Criteria

  • From 21-50 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 all ceramic crowns in esthetic zone;
  • Badly decayed teeth
  • Teeth restored with large filling restorations
  • Endodontically treated teeth
  • Malformed teeth
  • Malposed teeth (Tilted, over-erupted, rotated, etc.)
  • Able to return for follow-up examinations and evaluation.

Exclusion Criteria

  • Patient less than 21or more than 50 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 integrity

Time Frame: 1 year

Measured by using Modified United States Public Health Service criteria (USPHS criteria) * Alpha (A) the explorer does not catch when drawn across the surface of the restoration toward the tooth, or, if the explorer does not catch, there is no visible crevice along the periphery of the restoration (visual inspection explorer) * Bravo (B) the explorer catches and the is visible evidence of the crevice, which the explorer penetrates, indicating that the edge of the restoration does not adapt closely to the tooth structure. The dentin and/or the base is not exposed, and the restoration is not mobile ( visual inspection and explorer) * Charlie (C) the explorer penetrates crevice defect extended to the dento-enamel junction (explorer)

Secondary Outcomes

  • Gingival inflammation(1 year)
  • Secondary caries(1 year)
  • Restoration color stability(1 year)
  • Gingival discoloration(1 year)
  • patient satisfaction(1 year)

Study Sites (1)

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