Actively Recruiting

Phase Not Applicable
Age: 21Years +
All Genders
NCT07017062

Clinical Evaluation of Hybrid Ceramic Occlusal Veneers Bonded With Two Self Adhesive Resin Cements

Led by Cairo University · Updated on 2025-06-12

44

Participants Needed

1

Research Sites

82 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This randomized clinical trial aims to evaluate the clinical performance of hybrid ceramic occlusal veneers cemented with two different bonding protocols: a self-adhesive bonding protocol with adhesive enhancement (BeautiLink SA cement with BeautiBond Xtreme adhesive) versus another self-adhesive bonding protocol (RelyX U200 self-adhesive resin cement with 3M UNIVERSAL bond).

CONDITIONS

Official Title

Clinical Evaluation of Hybrid Ceramic Occlusal Veneers Bonded With Two Self Adhesive Resin Cements

Who Can Participate

Age: 21Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 21 years or older
  • Vital teeth
  • Sufficient tooth structure for veneer retention
  • Willing and able to provide written informed consent
  • Ability to attend all follow-up appointments
  • Adequate oral hygiene as determined by the investigator
Not Eligible

You will not qualify if you...

  • Active periodontal disease with probing depth greater than 4mm or bleeding on probing
  • Severe parafunctional habits such as bruxism confirmed by clinical examination
  • Poor oral hygiene with plaque index greater than 30%
  • Pregnancy or nursing
  • Systemic diseases affecting treatment outcomes such as uncontrolled diabetes or immunosuppression
  • Known allergies to ceramic or resin cement components
  • Inability to comply with study requirements
  • Current participation in other dental clinical trials
  • Active orthodontic treatment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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

H

Hayat Ibrahim El Banna, Lecturer

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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