Status:

UNKNOWN

Clinical Evaluation of Wear Behavior of Human Enamel and Chipping of Veneered Zirconia Against Monolithic Zirconia

Lead Sponsor:

Cairo University

Conditions:

Broken Tooth With Complication

Non Vital Teeth

Eligibility:

All Genders

20-60 years

Phase:

NA

Brief Summary

The aim of this study is to evaluate chipping and the degree of natural enamel loss opposing to monolithic zirconia compared to veneered zirconia restoration.

Detailed Description

While increase using of zirconia in extra coronal restoration as a substitute for metal ceramic restoration still high rate of technical complications specifically chipping of veneering ceramic and we...

Eligibility Criteria

Inclusion

  • Age range of the patients from 20-60 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 (e.g. Moderate to severe discoloration, coronal fracture where partial coverage would lack retention, malposed or malformed teeth).
  • Patients with root canal treated teeth requiring full coverage restorations.
  • Patients willing to return for follow-up examinations and evaluation.

Exclusion

  • Patients in the growth stage with partially erupted teeth.
  • Patients with poor oral hygiene and motivation.
  • A pregnant woman'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 (patient that has phobia from dental treatments or needle bunch).
  • Patients have no opposite occluding dentition in the area intended for restoration.
  • Patients suffer from Para functional habits.

Key Trial Info

Start Date :

November 1 2017

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

February 1 2019

Estimated Enrollment :

26 Patients enrolled

Trial Details

Trial ID

NCT03295513

Start Date

November 1 2017

End Date

February 1 2019

Last Update

September 28 2017

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