Menu
Recruiting NCT07017062

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

No phase Interventional Occlusal Wear of Teeth

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: hybrid ceramic occlusal veneers.
Who it may be relevant to
Registry conditions: Occlusal Wear of Teeth. Basic parameters: from 21 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

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

Overview

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).

Interventions

  • Other hybrid ceramic occlusal veneers
    occlusal veneers cemented with self adhesive resin cements

Primary outcome measures

  • Marginal discoloration [Time frame: 18 months]
Secondary outcome measures (4)
  • Retention [Time frame: 18 months]
  • Marginal adaptation [Time frame: 18 months]
  • Postoperative hypersensitivity [Time frame: 18 months]
  • Recurrent caries [Time frame: 18 months]

Eligibility criteria

Inclusion criteria

  • • Age ≥ 21 years
  • 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

Exclusion criteria

  • • Patients with active periodontal disease (probing depth > 4mm, bleeding on probing)
  • Patients with severe parafunctional habits (e.g., bruxism confirmed by clinical examination)
  • Poor oral hygiene (plaque index > 30%)
  • Pregnancy or nursing
  • Systemic diseases affecting treatment outcomes (e.g., uncontrolled diabetes, immunosuppression)
  • Known allergies to study materials (ceramic, or resin cement components)
  • Inability to comply with study requirements
  • Current participation in other dental clinical trials
  • Active orthodontic treatment

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Faculty of Dentistry, Cairo University — Cairo

Identifiers

NCT: NCT07017062 · 2010777

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗