ConditionOcclusal Wear of Teeth
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 groupsSponsors and collaborators
Source ClinicalTrials.gov