Clinical Performance of Hybrid Ceramic Laminate Veneers

Recruiting N/A Interventional Study
Bonding of Veneers After Different Treatment
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
21 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
28 (estimated)
Sponsor
Cairo University · Other
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About This Trial

This randomized controlled trial evaluates the clinical performance of laminate veneers fabricated from HC hard blocks pretreated with BeautiBond Xtreme versus HC Primer, using BeautiLink SA cement. The study focuses on marginal adaptation, retention, discoloration, and recurrent caries over 18 months.

Trial Locations
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Eligibility Criteria
Inclusion Criteria:dult patients ≥ 21 years requiring laminate veneers in the esthetic zone, vital or endodontically treated teeth, sufficient enamel, willing and able to consent and comply. \- Exclusion Criteria: Periodontal disease, bruxism, poor hygiene, pregnancy, systemic illness, allergies, …
Contacts

omnia Mohammed Wafik, lecturer

00201006595375

omniawafik@gmail.com

CONTACT