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.

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age21-50
SponsorCairo University

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 volunteers

Qualifiers

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

Design model

Parallel

Treatments tested in this trial

  • Resin Cement

    Other intervention

    Bioactive self adhesive resin cement (SHOFU BeautiLink) used to cement indirect restorations to endodontically treated molars.

  • Resin Cement

    Other intervention

    Self adhesive resin cement

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: Indirect Restorations cemented using Coltene Solocem Resin CementActive comparator 1 intervention
Group B: Indirect Restorations cemented using SHOFU BeautiLink Resin CementActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Modified USPHS Criteria

Time frame
2 years

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: