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

Cairo University (CU)

Status

Enrolling

Conditions

Occlusal Wear of Teeth

Treatments

Other: hybrid ceramic occlusal veneers

Study type

Interventional

Funder types

Other

Identifiers

NCT07017062

2010777

Details and patient eligibility

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).

Enrollment

44 estimated patients

Sex

All

Ages

21+ years old

Volunteers

No Healthy Volunteers

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