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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age21+
SponsorCairo University

About this trial

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).

Eligibility criteria

Qualifiers

• Age ≥ 21 years

Vital teeth

Sufficient tooth structure for veneer retention

Willing and able to provide written informed consent

Disqualifiers

• 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

Trial design

Treatments tested in this trial

  • hybrid ceramic occlusal veneers

Treatment groups

44 Participants
are divided into 2 treatment groups

Sponsors and collaborators