Comparative clinical evaluation of different tooth colored filling materials
- Conditions
- Health Condition 1: K025- Dental caries on pit and fissure surface
- Registration Number
- CTRI/2023/06/053890
- Lead Sponsor
- ANDURI N S R L SRI NAVYA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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)
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
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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. <br/ ><br> <br/ ><br>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. <br/ ><br>Timepoint: 3 months follow up, USPHS Criteria
- Secondary Outcome Measures
Name Time Method Evaluation of 3 month post-operative sensitivity in Class I cavities restored with Sonicfill delivery system and Surefil composite activated using SmartLite Pro EndoActivator. <br/ ><br>Timepoint: 3 months follow up, USPHS criteria