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

NCT ID: NCT07017062

Last Updated: 2025-06-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

44 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-06-30

Study Completion Date

2027-01-31

Brief Summary

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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).

Detailed Description

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Conditions

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Occlusal Wear of Teeth

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Hybrid ceramic occlusal veneers cemented with Rely X U200 cement

Group Type ACTIVE_COMPARATOR

hybrid ceramic occlusal veneers

Intervention Type OTHER

occlusal veneers cemented with self adhesive resin cements

Hybrid ceramic occlusal veneers cemented with BeautiLink SA cement

Group Type EXPERIMENTAL

hybrid ceramic occlusal veneers

Intervention Type OTHER

occlusal veneers cemented with self adhesive resin cements

Interventions

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hybrid ceramic occlusal veneers

occlusal veneers cemented with self adhesive resin cements

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

21 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Cairo University

OTHER

Sponsor Role lead

Responsible Party

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Hayat Ibrahim Mahrous Ibrahim

principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Faculty of Dentistry, Cairo University

Cairo, , Egypt

Site Status RECRUITING

Countries

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Egypt

Central Contacts

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Hayat Ibrahim El Banna, Lecturer

Role: CONTACT

00201001248734

Facility Contacts

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Faculty of Dentistry, Cairo University

Role: primary

00201002159535

Other Identifiers

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2010777

Identifier Type: -

Identifier Source: org_study_id

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