Comparison of the Clinical Performance of High Strength Hybrid Ceramic Indirect Restorations Cemented on Endodontically Treated Teeth Using Bioactive Versus Conventional Self Adhesive Resin Cements.
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Resin Cement, Resin Cement.
- Who it may be relevant to
- Registry conditions: Endodontically Treated Molar. Basic parameters: 21 years — 50 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Clinical Performance of CAD/CAM Hard Hybrid Ceramic Overlays on Endodontically Treated Molars Using Bioactive Versus Conventional Self-Adhesive Resin Cement: Two-Year Randomized Clinical Trial
Overview
Cementation of indirect restoration is a determinant of the success or failure of the fabricated restoration and consequentially the entire tooth. While there are numerous commercially available resin cements in the dental market, not all have been sufficiently assessed with significant follow up periods to clinically determine their success or failure. As such, this research will be conducted to elucidate if there is a viability to the cementation of indirect hybrid ceramic blocks over endodontically treated teeth using bioactive self-adhesive resin cement and determining whether it provides a clinical advantage and improved restoration serviceability in the oral cavity.
Interventions
- Other Resin Cement
Bioactive self adhesive resin cement (SHOFU BeautiLink) used to cement indirect restorations to endodontically treated molars. - Other Resin Cement
Self adhesive resin cement
Primary outcome measures
- Modified USPHS Criteria [Time frame: 2 years]
Eligibility criteria
Inclusion criteria
- Patient Related Criteria:
- Adult patients (age: 21-50 years) of both genders.
- Able to tolerate necessary restorative procedures.
- Willing to sign the informed consent.
- Accepts the follow-up period.
Tooth Related Criteria:
- Endodontically treated first and second permanent molars.
- Access cavities with one missing proximal wall i.e. Occluso-mesial/distal cavities
- Patients with proper oral hygiene
Exclusion criteria
- Endodontically treated anterior, premolar and third molar teeth
- Badly broken-down teeth
- Hopelessly carious/destructed teeth necessitating extraction
- Mobile teeth, indicating periodontal disease or trauma.
- External or internal resorption.
- Cervical carious lesions
- Medically compromised patients
- Patients with known allergies to Latex and/or resinous material
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Quadruple blind
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06787469 · ANCU-8-1-2025