About this trial
Using bioactive injectable resin composite in anterior class v carious lesions can provide better aesthetic outcome and marginal integrity by releasing multiple ions, including fluoride. This offers better marginal integrity due to presence of S-PRG fillers
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Age 20-60 years.
Co-operative participants approving to participate in the study.
Male or female patients.
Medically free participants.
Disqualifiers
Systemic disease or severe medical complications.
Participants with a history of allergy to any component of restorations will be used in the study.
Lack of compliance
Evidence of severe bruxism, clenching, or temporomandibular joint disorders or bizarre habits
Trial design
Parallel
Treatments tested in this trial
Giomer based injectable composite
Procedure/SurgeryGiomers utilize surface pre-reacted glass (SPRG) technology, which involves an acid-base reaction between fluorine-containing glass particles and polymer-containing acid when exposed to water. This reaction results in the formation of a glass ionomer phase, which is then dispersed throughout the resin. Furthermore, the S-PRG fillers present in giomer materials enable the continuous release and replenishment of fluoride, offering long-lasting protection against the recurrence of caries
Universal injectable resin composite
Procedure/SurgeryConventional injectable resin composite
Treatment groups
Trial outcomes
Primary outcomes
Marginal discoloration using FDI criteria
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: