Health Condition 1: K025- Dental caries on pit and fissure surface
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients willing to provide voluntary written informed consent Patients in good medical health and able to tolerate the dental procedures Has at least 1 molar that require Class I restoration. Study teeth must be in occlusal function. Study teeth must be vital (i.e., free of clinical signs and symptoms of periapical pathology)
Exclusion criteria
Exclusion criteria: Patient currently taking part in an evaluation of other dental restorative materials Teeth exhibiting clinical signs of periapical pathology Teeth with a history of self-reported preoperative pulpal problems Known allergy to resin composites. Abnormal oral soft tissue findings (e.g., open sores, lesions) Are unwilling or unable to have dental radiographs or photographs taken of their dentition and soft tissues
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.To evaluate 3 month clinical retention, color match, marginal discoloration, marginal adaptation, secondary caries, surface texture, anatomic form, in Class I cavities restored with Sonicfill composite delivery system. 2. To evaluate 3 month clinical retention, color match, marginal discoloration, marginal adaptation, secondary caries, surface texture, anatomic form, in Class I cavities restored with Surefil composite activated using SmartLite Pro EndoActivator. Timepoint: 3 months follow up, USPHS Criteria | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluation of 3 month post-operative sensitivity in Class I cavities restored with Sonicfill delivery system and Surefil composite activated using SmartLite Pro EndoActivator. Timepoint: 3 months follow up, USPHS criteria | — |
Countries
India
Contacts
Sibar Institute of dental sciences