Actively Recruiting

Phase Not Applicable
Age: 21Years +
All Genders
NCT07043998

Evaluation of Full Veneered Porcelain-Fused-to-Metal Crowns Cemented With Self-Adhesive Resin Cement Using Two Curing Modes

Led by Cairo University · Updated on 2025-06-29

54

Participants Needed

1

Research Sites

108 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

P - Population/Patient Problem Adult patients requiring full coverage porcelain-fused-to-metal (PFM) crown restorations I - Intervention PFM crowns veneered with porcelain system cemented using self-adhesive resin cement in DUAL-CURED mode (light-cured for 20 seconds per surface) C - Comparison PFM crowns veneered with porcelain system cemented using self-adhesive resin cement in SELF-CURED mode (no light curing, 5 minutes self-cure) O - Outcome(s) * Primary: Retention of PFM crowns (Modified USPHS criteria) * Secondary: Marginal adaptation, recurrent caries, marginal discoloration (Modified USPHS criteria) T - Time 18-month follow-up period with evaluations at baseline, 6, 12, and 18 months

CONDITIONS

Official Title

Evaluation of Full Veneered Porcelain-Fused-to-Metal Crowns Cemented With Self-Adhesive Resin Cement Using Two Curing Modes

Who Can Participate

Age: 21Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients requiring full coverage PFM crown restorations
  • Age 21 years or older
  • Teeth that are vital or have had root canal treatment
  • Sufficient tooth structure to retain the crown
  • Willing and able to provide written informed consent
  • Ability to attend all follow-up visits
  • Adequate oral hygiene as assessed by the investigator
Not Eligible

You will not qualify if you...

  • Active periodontal disease with probing depth over 4 mm or bleeding on probing
  • Severe parafunctional habits like bruxism confirmed by clinical exam
  • Poor oral hygiene with plaque index over 30%
  • Pregnancy or nursing
  • Systemic diseases that could affect treatment results, such as uncontrolled diabetes or immunosuppression
  • Known allergies to metal alloys, porcelain, or resin cement components used in the study
  • Inability to follow study requirements
  • Currently enrolled in other dental clinical trials
  • Active orthodontic treatment

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Faculty of Dentistry Cairo University

Cairo, Egypt

Actively Recruiting

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Research Team

O

Omnia Nabil, Associate Professor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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