About this trial
The objective of this study is to evaluate the micro-tensile bond strength of a newly self-adhesive resinous restorative material to dentin with and without application of universal bonding system (in-vitro) and to examine it's clinical performance by evaluation of it's color stability and marginal discoloration through a randomized clinical trial (in-vivo).
Eligibility criteria
Qualifiers
Patients with class I lesion in their maxillary or mandibular molars with a maximum of approximately 2 mm final cavity depth.
Patients with teeth shade A2 according to Vitapan classical shade guide.
Patients with an acceptable oral hygiene level.
Patients keen to regularly attend the follow up visits.
Disqualifiers
Patients with heavy bruxism or traumatic occlusion.
Patients with poor oral hygiene or active periodontal disease.
Patients with exposed or endodontically treated teeth.
Patients participated in a clinical trial within 6 months before beginning of this trial.
Trial design
Treatments tested in this trial
- self-adhesive resin restoration