Status:

UNKNOWN

Gingival Inflammatory Response,Bacterial Adhesion and Patient Satisfaction of Ceramo-metallic vs Zirconia Crowns

Lead Sponsor:

Cairo University

Conditions:

Gingival Inflammation

Oral Bacterial Infection

Eligibility:

All Genders

20-50 years

Phase:

NA

Brief Summary

Ceramo metallic restoration has proved high success rate over past years as considered to be the gold standard while Monolithic zirconia as fixed dental prostheses have gained attention because of the...

Detailed Description

For years, the ceramo-metal restoration has been the gold standard in crown and bridge procedures .They have been used for many years and studied extensively. Studies have demonstrated a 94% success r...

Eligibility Criteria

Inclusion

  • inclusion criteria
  • Patient age range from 20-50 to be able to read and write in order to sign the informed consent document.
  • Patients physically and psychologically able to tolerate conventional restorative procedures.
  • Patients with no active periodontal and or pulpal diseases, having teeth with good restorations.
  • Patients with root canal treated teeth requiring full coverage restorations.
  • Patients indicated for full coverage (e.g. moderate to severe discoloration, coronal fracture).
  • Patients didn't take antibiotics or anti-inflammatory in the past three months.
  • Surfaces with an adjacent probing pocket depth exceeding 3mm were not included
  • Patients willing to return for follow-up examinations and assessments.
  • Exclusion criteria:
  • Patients in the growth stage with partially erupted teeth.
  • Patient with poor oral hygiene.
  • Patients with psychiatric problems or unrealistic expectations
  • Patient with no opposite occluding dentition in the area intended for restoration.
  • Patient suffering from Para functional habits.
  • Patient with diabetes mellitus, hypertension and gingivitis or periodontitis which has impact on gingival cervicular fluid level

Exclusion

    Key Trial Info

    Start Date :

    November 1 2019

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ESTIMATED

    End Date :

    December 1 2021

    Estimated Enrollment :

    20 Patients enrolled

    Trial Details

    Trial ID

    NCT04077606

    Start Date

    November 1 2019

    End Date

    December 1 2021

    Last Update

    September 4 2019

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