Color Stability and Wear Resistance of Direct Flowable and Preheated Composite Using the Injectable Technique
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorKing Abdullah University Hospital
About this trial
The aim of this study is to conduct the first clinical trial to assess the color stability and wear resistance of the highly filled injectable flowable composite materials compared to preheated conventional ones and evaluate the in vivo performance of the injectable composite technique.
Eligibility criteria
Qualifiers
Patients older than 18 years
Asymptomatic sound anterior teeth, or localized Class III/IV/V cavity or restoration
Patients with irregular tooth anatomies, misalignments, spacing, mild staining, cervical wear that are indicated for direct composite veneers
Restorations in functional occlusions with an opposing natural tooth.
Disqualifiers
Patients with contra-indications for regular dental treatment based on their medical history.
Patients at a high risk of caries.
Patients with poor oral hygiene.
Teeth with compromised periodontal status.
Trial design
Treatments tested in this trial
- Experimental: Group1: Estelite Sigma Quick
- Experimental: Group 2: Estelite Flow Quick
Treatment groups
142 Participants
are divided into 2 treatment groupsSponsors and collaborators
King Abdullah University Hospital
Lead sponsor
Jordan University of Science and Technology
Collaborator
Source ClinicalTrials.gov