About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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.
Disqualifiers
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.
Trial design
Parallel
Treatments tested in this trial
Resin Cement
Other interventionBioactive self adhesive resin cement (SHOFU BeautiLink) used to cement indirect restorations to endodontically treated molars.
Resin Cement
Other interventionSelf adhesive resin cement
Treatment groups
Trial outcomes
Primary outcomes
Modified USPHS Criteria
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: