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

Recruiting now · Not applicable

Conditions studied: Occlusal Wear of Teeth

In brief

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).

Key facts

Study ID

NCT07017062

Run by

Cairo University

People needed

44

Starts

2025-06-01

Expected to finish

2027-01-01

Last updated by the study team

2025-06-12

Who can join

Age: 21 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• • 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

You may not qualify if…

• • 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

Where it is running

• Faculty of Dentistry, Cairo University — Cairo, Egypt (enrolling)

Full record on ClinicalTrials.gov

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